SAS Jobs

Senior / Principal SAS Programmer - PRA International (Lenexa, KS)

2008-06-05T23:25:00.000-07:00

* Relocation assistance provided *

We are currently seeking experienced Statistical SAS Programmers for our growing Analysis & Reporting teams. Several levels are available...including TEAM LEAD / PRINCIPAL positions.

Our SAS Programmers provides statistical programming support and validation of statistical analyses, datasets, tables, figures and listings. Additionally, these individuals also provide statistical output for clinical study reports.

The Senior SAS Programmer will:

Review clinical study protocols and case report forms
Work with biostatisticians, writers and clinical staff to generate data summarization, analysis and reports
Write and document programs
Write command files
Generate analysis databases in SAS
Produce tables, listings and plots presenting data
Review reports for consistency between text and tables
Perform ad hoc programming
May mentor new and/or junior-level programmers

The Principal SAS Programmer will:

Provide senior-level statistical programming support
Serve as the Project Team Leader overseeing operational activities of the other Analysis Programmers
Provide validation of statistical analyses, datasets, tables, figures and listings
Participate in the implementation / testing of new software applications
Contribute to the review and update of SOPs
Lead new business initiatives

QUALIFICATIONS

Bachelors degree in Statistics or Biostatistics (or comparable) is required; and advanced degree (M.S. or Ph.D.) is preferred
A minimum of 2 years of SAS programming experience (for a Sr. Programmer role) and 5 – 7 years of SAS programming experience (for a Principal Programmer role) – in a clinical trial setting
Previous experience working in a pharmaceutical company or contract research organization (CRO) is required
Strong experience using computerized systems – particularly SAS® programming
Superior oral / written communication and presentation skills
As a Principal SAS Programmer – you must have the demonstrated ability to plan, supervise, implement, and monitor the Statistical SAS Programming processes for multiple clinical trials

Website: http://www.prainternational.com/careers.htm
Contact: WaerhouseAimee [at] praintl.com

With more than 3,000 employees on six continents and over 25 years in business, PRA International has distinguished itself as one of the Top 10 international clinical research organizations (CROs) in the drug development industry. In 2006, we were ranked #48 in Forbes Magazines Top 200 Small Companies in America. We are the ONLY Clinical Research Organization to make it onto this list.

PRA International provides employees the opportunity to work on complex, global trials that can change the course of medicine. PRA has a single mission…to be the best clinical development organization in the world. Strategically aligned with leading pharmaceutical and biotech companies worldwide, we provide a broad array of services that encompass the entire spectrum of clinical development and work on some of the most advanced drugs and biologics in development today.

In addition to a unique professional challenge, PRA adheres to a pay-for-performance compensation philosophy, a commitment to professional development, and a culture that encourages a work/life balance.

PRA International also offers:

Extended personal time off – 4 weeks of Paid Time Off your first year; 5 weeks after three years; 6 weeks after five years
Competitive benefits plan – including Annual Bonus Plan
FLEXIBLE work schedules
Access to world-class therapeutic expertise – unrivaled by any other CRO

URL: www.datashaping.com/jobs17294x.shtml
Please mention datashaping.com when applying. Thank you.

Senior / Principal SAS Programmer - PRA International (Raleigh, NC)

2008-06-05T23:24:00.000-07:00

* Relocation assistance provided *

We are currently seeking experienced Statistical SAS Programmers for our growing Analysis & Reporting teams. Several levels are available...including TEAM LEAD / PRINCIPAL positions.
Our SAS Programmers provides statistical programming support and validation of statistical analyses, datasets, tables, figures and listings. Additionally, these individuals also provide statistical output for clinical study reports.
The Senior SAS Programmer will:

Review clinical study protocols and case report forms
Work with biostatisticians, writers and clinical staff to generate data summarization, analysis and reports
Write and document programs
Write command files
Generate analysis databases in SAS
Produce tables, listings and plots presenting data
Review reports for consistency between text and tables
Perform ad hoc programming
May mentor new and/or junior-level programmers

The Principal SAS Programmer will:

Provide senior-level statistical programming support
Serve as the Project Team Leader overseeing operational activities of the other Analysis Programmers
Provide validation of statistical analyses, datasets, tables, figures and listings
Participate in the implementation / testing of new software applications
Contribute to the review and update of SOPs
Lead new business initiatives

QUALIFICATIONS

Bachelors degree in Statistics or Biostatistics (or comparable) is required; and advanced degree (M.S. or Ph.D.) is preferred
A minimum of 2 years of SAS programming experience (for a Sr. Programmer role) and 5 – 7 years of SAS programming experience (for a Principal Programmer role) – in a clinical trial setting
Previous experience working in a pharmaceutical company or contract research organization (CRO) is required
Strong experience using computerized systems – particularly SAS® programming
Superior oral / written communication and presentation skills
As a Principal SAS Programmer – you must have the demonstrated ability to plan, supervise, implement, and monitor the Statistical SAS Programming processes for multiple clinical trials

Website: http://www.prainternational.com/careers.htm
Contact: WaerhouseAimee [at] praintl.com

PRA International also offers:

Extended personal time off – 4 weeks of Paid Time Off your first year; 5 weeks after three years; 6 weeks after five years
Competitive benefits plan – including Annual Bonus Plan
FLEXIBLE work schedules
Access to world-class therapeutic expertise – unrivaled by any other CRO

URL: www.datashaping.com/jobs17295x.shtml
Please mention datashaping.com when applying. Thank you.

Senior SAS Analyst - NYC Dept. of Education (New York, NY)

2008-04-20T21:38:00.002-07:00

The The New York City Department of Education is hiring a Senior Analyst (SAS), Data Management. The complete job description is posted at http://schools.nyc.gov/Offices/DHR/CareerOpportunities/ under the Chancellor's Accountability Initiative. Or if you e-mail me directly, I will send you a word document with the posting. I strongly recommend anyone interested apply, as the DOE is great work environment and engaged in a number of exciting projects. Applicants can apply online (preferable) or email Cassandra Johnson at CRJohns@schools.nyc.gov .

Job Description

Position Summary: The New York City Department of Education is the largest school system in the nation, with nearly 1.1 million students, 135,000 employees (including 80,000 teachers) and an annual budget of $14+ billion. Led by Schools Chancellor Joel I. Klein, the Department of Education (DOE) is committed to creating a system of 1,400+ great schools. Since its inception in 2003, the Children First Agenda for New York's schools has driven the Department of Education's work in adopting uniform, rigorous curricula for all schools, starting new small schools to increase educational options for students and transforming the structure and culture of the Department of Education to encourage educational excellence and the work necessary to support that goal.

Working with the Associate Director, Data Management and other project team members, the Senior Analyst work focuses heavily on confidential data analysis, developing Quality Assurance (QA) rules for student and school level data and performing QA. The Senior Analyst will also streamline the data cleansing needs throughout the DOE. It also involves the handling the provision of confidential city and state accountability data

Reports to: Associate Director, Data Management

Direct Reports: N/A

Key Relationships: Will work closely with other members of the data management team, the Evaluation and Reporting the ARIS team, and the Periodic Assessments team.

RESPONSIBILITIES

Manage the utilization of confidential data (Student level data - Names, DOB, Gender, Ethnicity, Test and Assessment Data) associated with providing senior leadership staff with a continuous stream of information and analysis in support of the policy discussion-making process for all initiatives in the Office of Accountability. This will entail:
Develop operational SAS code based on predetermined business rules for DOE Reports.
Create standard and ad hoc queries to pull data from OA's internal databases and other NYC Department of Education data sources to analyze the metrics used to identify Schools in Need if Improvement (SIN) and Non-SINI and analyze and improve the metrics used to identify A-F schools for city and state accountability.
Create standard and ad hoc queries to pull data from OA's internal databases and other NYC Department of Education data sources to identify the demonstrated capacities of each such school to improve the ELA, math, science, and social studies outcomes of all students and particular target populations of students (e.g., Special Education, English Language Learners, other NCLB categories, students in bottom one-third of performers at the school and citywide).
Perform data cleansing and data verification at the school level when needed.
Utilize data analysis to prepare policy recommendations that include,
Creating and maintaining a data quality model for the DOE
Developing processes that ensure the integrity and accuracy of the source system data at point of entry
Developing processes that ensure the accuracy of similar data sets across disparate source systems
Develop standard reports that can be used by principals, school network management, school support organizations, and central NYC Department of Education staff to make informed decisions regarding improved outcomes for all students and particular groups of students.

QUALIFICATIONS Minimum Requirements

A Baccalaureate degree from an accredited college in finance, accounting, operations research, business or public administration, or a closely related and three (3) years of satisfactory full-time professional experience in budget administration, economic or financial administration, fiscal, operations or economic research; management or methods analysis, educational or public administration, economic planning, fiscal management, or a related area.
A baccalaureate degree from an accredited college and at least three years of full-time, paid experience in data analysis, education administration, evaluation and testing, educational planning, or statistics or a master's degree and at least one year of work experience in the above fields.

PLUS

Expert level ability in SAS Proficiency in other Microsoft Office software applications.

Preferred

Superior analytical skills and comprehensive knowledge of best practices in research and evaluation.
Project management and process improvement skills.
Experience with Microsoft SQL2000 and knowledge of SQL tools/management techniques.
Knowledge of IBM Mainframe,TSO/ISPF, OS JCL
Strong Excel and Access skills
Creative problem solving ability with the facility to perform independent, thoughtful analysis around important educational issues.
Excellent organization and interpersonal skills in dealing with administrative and school-based personnel.
Capacity to work under pressure and effectively prioritize in a demanding environment.
Demonstrated interest and experience in education and public policy a plus.
Microsoft Access, Visual Basics for Application.

Salary: $65,120+

Please include cover letter with your application.

Resumes will be reviewed on an ongoing basis. We encourage applicants to apply as soon as possible.

NOTE: The filling of all positions is subject to budget availability.

AN EQUAL OPPORTUNITY EMPLOYER

It is the policy of the Department of Education of the City of New York to provide educational and employment opportunities without regard to race, color, religion, creed, national origin, alienage and citizenship status, age, marital status, disability, prior record of arrest or conviction (except as provided by law), sexual orientation, gender (sex), and to maintain an environment free of discriminatory harassment, including sexual harassment, or retaliation as required by civil rights law. Inquiries regarding compliance with this equal opportunity policy may be directed to: Office of Equal Opportunity, 65 Court Street, Room 923, Brooklyn, New York 11201, or visit the OEO website at 'http://schools.nyc.gov/Administration/Offices/GeneralCounsel/OEO/default.htm.'

URL: www.datashaping.com/jobs17239f.shtml
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SAS Developer, contract (Richmond, VA)

2008-04-20T21:38:00.001-07:00

Req. ID: 16294 Position Title: SAS Developer
Contact Name: Smith Sheik (smith@vls-systems.com)
Location: Richmond VA
Duration: 6-12 months
Required Skills: SAS Macro language ,SQL , Oracle
Job Description:

Face to Face a must,H1B transfers/EAD/GC/Citizens

Contributes to development and directs task identification, work effort estimates, and work schedules for development and maintenance activities.
Participates in and may direct problem definition and problem resolution activities.
Participates in and may direct the analysis and definition of efficient, cost effective application solutions which support client business processes and functional requirements.
Coordinates with internal departments to provide associated deliverables required for the successful completion of development and maintenance assignments (e.g. database development, job scheduling, CICS support, network support, help desk orientation, client implementation readiness, etc.).
Conducts client interviews in order to perform analysis of client business processes and functional requirements and prepares appropriate documentation to communicate and validate the information.
May participate in client committees and may coordinate client involvement in development and maintenance tasks as needed.
May prepare and conduct presentations of various work products.
Provides on call support and may coordinate on call response efforts as assigned.

Position Requirements:

5-6 years programming in SAS and the SAS Macro language in a Unix environment
Proficiency in SQL and Oracle databases
Bachelor's degree in Computer Science or related field or equivalent experience.
Demonstrated excellence in technical skills and technical knowledge required in one or more higher level programming languages respective to various mainframe or client server programming development environments.
Strong skills required in critical thinking and analysis, verbal and written communications, and interpersonal interactions (e.g. partnering, conflict manageme! nt, cons ulting, etc.).
Understanding of health care business and care delivery processes preferred.

URL: www.datashaping.com/jobs17166f.shtml
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SAS Statistician / Data Mining - CDC (Atlanta, GA)

2008-04-20T21:37:00.001-07:00

Staff STATISTICIAN (Fulltime, On-SITE)
Location: Atlanta, Georgia
Project: Vaccine Analytic Unit

The Meningitis and Vaccine Preventable Diseases Branch (MVPDB), located within the Division of Bacterial Diseases (DBD) of the National Center for Immunization and Respiratory Diseases (NCIRD) is collaborating with the Department of Defense (DoD) and FDA on a series of studies to investigate the longer term safety of anthrax vaccine and other vaccines currently administered in DoD. This position will provide the opportunity to be part of a multi-agency working group actively involved in cutting edge research relevant to bioterrorism preparedness and vaccine development.

Scope of Work:

The main duties for this position are to participate in ongoing post- marketing surveillance studies with particular focus on data mining applications for conducting more real time surveillance for adverse events following immunizations using the DoD Defense Medical Surveillance System (DMSS) database. The incumbent would be expected to work with the current VAU statistician and programmer and other staff in the design, initiation, and implementation of complex epidemiologic studies and analyses. The incumbent would be asked to assist with all aspects of epidemiological research including: development, implementation, data management, data analysis and report/publication preparation. Travel to Washington, D.C. (approximately 4 - 6 trips per year) will be necessary and the incumbent may be asked to attend off-site scientific meetings.

Position Requirements:

A combination of a Master's of Science Degree (or equivalent) and 5 years of experience or a PhD and 3 years of experience that provides the knowledge, skills and abilities necessary for acceptable job performance is necessary. A minimum of two years experience using data mining methods on large linked databases is desirable. Candidates should have experience working with epidemiologic research studies, managing large linked databases and writing project reports or research protocols, as well as excellent SAS programming skills. Due to the consultative nature of this position, a candidate must also have excellent communication skills.

Apply Online

URL: www.datashaping.com/jobs17230e.shtml
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SAS Clinical Programmer (La Jolla, CA)

2008-04-20T21:36:00.000-07:00

Relocation assistance may be available.

Please respond to: joe [at] g-2-consulting.com

Responsibilities:

Position Purpose:

Role is primarily responsible for the project lead of statistical programming actives in the Clinical Programming group. SAS programming is a core skill, but main focus of the position is oversight of external providers performing programming.

Accountable for the provision of standard and non-standard data sets, tables, listings and figures based on the final synopsis and SAP that are required for the study reports, submissions and product defense
Delivers against the overall protocol timeline, cost and quality goals through matrix communication within the Study Team
Clearly specifies requirements to external resources and to assure the quality of deliverables provided by external resources
Champions operational excellence to provide continuous improvement of processes and sharing of best practices across TAs
Tracks milestones against project timelines
Communicates effectively not only within the teams and functional lines but also with the external resources

Major Duties:

Serve as the clinical programming representative on drug development project teams, working closely with project team leaders and CPW leadership to establish strategy, time lines, and project management for the analysis and reporting of clinical study data
Actively support the CPW Sourcing model where programming is primarily performed by Shanghai or FSP partners and overseen by Internal Programmers who are the face for the team. Accountable for the delivery of tables, listings and figures through FSP and low-cost providers
Makes decisions regarding operations within relevant therapeutic area, including project plans, specifications and resource allocation, allowing time and resource for ESUB activities
Oversee the development of standard and non-standard datasets, tables, listings, and figures based on the final protocol synopsis and SAP that are required for the clinical study report, submissions and product defense
Adhere to TA standards, aligning phase I to IV programming standards to develop repositories to support enhanced clinical trials, safety first initiative, commercial and litigation support
Prepare for an ESUB by ensuring that value added datasets and their programming plans meet the FDA's ESUB requirements as well as study reporting needs. Contribute to the production of ESUB components when required either directly, by providing additional information or by way of review
Provides filing, approval and regulatory programming support for all aspects of a submission
Aligns cross-functionally with project team members to address project- related goals
Provides end game report and IB tables, listings and figures

Qualifications:

Training & Education Preferred:

Minimum: BS in Statistics with 4 to 6 years relevant experience or equivalent experience
Desirable: MS in Statistics with 6 - 9 years industry experience or equivalent experience
At least 3 years experience with SAS
At least 3 years of statistical programming experience including the analysis and reporting of clinical trial data
At least 3 years experience working in a disciplined systems programming environment; experienced with Software Development Life cycle (SDLC) and regulatory validation requirements including 21 CFR Part 11

Prior Experience Preferred

Demonstrated knowledge of clinical development and regulatory submission processes
Expert knowledge of base SAS, SAS macro language, graph, FSP, AF, STATS, SQL as well as other programming languages, etc
Knowledge of FDA guidance on electronic submissions
Able to manage multiple projects simultaneously
Experience with SAS statistical procedures
Knowledge of systems testing processes and documentation
Strong interpersonal, verbal and written communication skills
Demonstrated ability to work collaboratively on multidisciplinary teams
Leadership, communication and project management skills required

URL: www.datashaping.com/jobs17228e.shtml
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SAS Clinical Programmers (New York, NY)

2008-04-20T21:35:00.002-07:00

We need several experienced people ( 2 years min for Jr role. # years min for Sr.) re: the following in NYC. Excellent Benefits are provided including 4 weeks paid time off 1st year and 5 weeks 2nd year.

Please respond to: joe [at] g-2-consulting.com

PRIMARY FOCUS

Produce data analysis sets, listings, tables, ad hoc reports and validates programming as required for the effective operation and completion of clinical studies.

SUMMARY

Under limited direction, responsible for the day-to-day development, maintenance and management of multiple clinical study databases and management of queries as requested by both internal and external sources and in compliance with FDA regulations and ICH guidelines.

ESSENTIAL DUTIES AND RESPONSIBILITIES

Designs clinical databases for clinical trials, writing database documentation, writing and performing database validation, creating data listings, ad hoc error detection methods and data displays.
Provides day-to-day oversight of assigned projects.
Conducts all aspects of data management (e.g., data entry, creation of datasets, edit checks, data cleaning, safety listings and data manipulation) utilizing given software and/or spreadsheet programs as necessary.
Reviews and contributes to the preparation of Case Report Forms (CRFs).
Develops query designs, standard tables for the presentation of data, analyses of data and reports as requested.
Responsible for developing and maintaining SAS standards for report quality tables, listings and figures, and report writing.
Keeps informed of SAS programming techniques as applied to clinical trials by reading relevant journals and/or attending courses/programming meetings.
Conducts regular testing and analysis of the database in order to maintain data integrity; performs quality review of SAS programs generated by other SAS programmers and biostatisticians.
Generates and updates program codes and data definitions as necessary.
Works with staff in developing research ideas suitable for publication.
Provides project guidance and instruction both internally and to study Sponsors regarding database design, implementation and database capabilities.
Communicates with internal departments and external organizations to facilitate data transfer.
Furnishes outcomes data to internal departments and external organizations as requested by supervisor.
Reports and collaborates with information technology consultants as necessary.
Participates in activities organized to improve operational activities of the department.
Additional duties as assigned.

QUALIFICATIONS

SAS Clinical Programmer - B.S. degree from an accredited institution in Computer Sciences or related programming courses or equivalent work experience; advanced degree preferred; a minimum 3 or more year(s) of experience in clinical database programming.
Senior SAS Clinical Programmer - B.S. degree from an accredited institution in Computer Sciences or related programming courses or equivalent work experience; advanced degree preferred; a minimum 5 or more year(s) of experience in clinical database programming.
Biomedical experience preferred.
Knowledge of medical and statistical terminology.
Knowledge and experience in implementing the GCP/ICH regulations and 21 CFR Part 11 preferred.
Familiarity and proficiency with computer programs including, but not limited to, Windows, Excel, MS Word and Outlook; working knowledge of MSaccess, Visual Basic, FileMaker Pro and relational databases desirable.
High level of proficiency in SAS.
Experience preparing study results for submission using SAS.
Familiarity with coding dictionaries.
Must possess excellent communication and writing skills, patience, professionalism and ability to effectively interact with staff and management alike; ability to verbally communicate effectively with data management, department clinical research and other team members.

URL: www.datashaping.com/jobs17226e.shtml
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Clinical SAS Programmer (Telecommute, UK)

2008-04-20T21:35:00.001-07:00

working FT from home

CONTRACT - Clinical SAS Programmer (working FT from home)
Position Type: Contract
Location: From home
Salary: GBP 40-45 per hour

Background:

My client is prepared to allow a Statistical Programmer the chance to provide services 100% from home. This role will run as a 3 month rolling contract and commence in May. The assignment will require the selected consultant to program derived datasets, tables, figures and listings independant of instruction and will ideally have a proven track record of successfully working from home.

Additional Information:

Hobson Prior is a specialist employment business acting on behalf of its client. We are a corporate member of the REC and operate strictly within the regulations governing the conduct of employment businesses which requires us to provide detailed information to candidates in relation to specific roles prior to the submission of their personal details and prohibits the disclosure of information relating to candidates without their consent. Hobson Prior is an accredited ISO9001:2000 business

To apply, please respond with an up to date CV quoting the reference: ' gv-9405 '. Alternatively, please contact me for further details

George Vernon
Hobson Prior
e: george.vernon [at] hobsonprior.com

URL: www.datashaping.com/jobs17182e.shtml
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Sr SAS Clinical Programmers (Hartford, CT)

2008-04-20T21:34:00.002-07:00

We urgently need 4 intermediate to Sr SAS Clinical Programmers with Pharmaceutical Industry experience. Description follows.

Please respond to: joe [at] g-2-consulting.com

Responsibilities:

Position Purpose:

Accountable for the provision of standard and non-standard data sets, tables, listings and figures based on the final synopsis and SAP that are required for the study reports, submissions and product defense
Delivers against the overall protocol timeline, cost and quality goals through matrix communication within the Study Team
Clearly specifies requirements to external resources and to assure the quality of deliverables provided by external resources
Champions operational excellence to provide continuous improvement of processes and sharing of best practices across TAs
Tracks milestones against project timelines
Communicates effectively not only within the teams and functional lines but also with the external resources

Major Duties:

Serve as the clinical programming representative on drug development project teams, working closely with project team leaders and CPW leadership to establish strategy, time lines, and project management for the analysis and reporting of clinical study data
Actively support the CPW Sourcing model where programming is primarily performed by Shanghai or FSP partners and overseen by Internal Programmers who are the face for the team. Accountable for the delivery of tables, listings and figures through FSP and low-cost providers
Makes decisions regarding operations within relevant therapeutic area, including project plans, specifications and resource allocation, allowing time and resource for ESUB activities
Oversee the development of standard and non-standard datasets, tables, listings, and figures based on the final protocol synopsis and SAP that are required for the clinical study report, submissions and product defense
Adhere to TA standards, aligning phase I to IV programming standards to develop repositories to support enhanced clinical trials, safety first initiative, commercial and litigation support
Prepare for an ESUB by ensuring that value added datasets and their programming plans meet the FDA's ESUB requirements as well as study reporting needs. Contribute to the production of ESUB components when required either directly, by providing additional information or by way of review
Provides filing, approval and regulatory programming support for all aspects of a submission
Aligns cross-functionally with project team members to address project-related goals
Provides end game report and IB tables, listings and figures

Qualifications:

Training & Education Preferred:

Minimum: BS in Statistics with 4 to 6 years relevant experience or equivalent experience. Desirable: MS in Statistics with 6 - 9 years industry experience or equivalent experience

At least 3 years experience with SAS
At least 3 years of statistical programming experience including the analysis and reporting of clinical trial data
At least 3 years experience working in a disciplined systems programming environment; experienced with Software Development Life cycle (SDLC) and regulatory validation requirements including 21 CFR Part 11

Prior Experience Preferred

Demonstrated knowledge of clinical development and regulatory submission processes
Expert knowledge of base SAS, SAS macro language, graph, FSP, AF, STATS, SQL as well as other programming languages, etc
Knowledge of FDA guidance on electronic submissions
Able to manage multiple projects simultaneously
Experience with SAS statistical procedures
Knowledge of systems testing processes and documentation
Strong interpersonal, verbal and written communication skills
Demonstrated ability to work collaboratively on multidisciplinary teams
Leadership, communication and project management skills required

URL: www.datashaping.com/jobs17181e.shtml
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Senior SAS Programmer Contract (Switzerland)

2008-04-20T21:34:00.001-07:00

World leading pharmaceutical, seeking experience SAS programmer with Clinical trials background a must. Pls contact me on 0044 (0)1273 727 930 or e-mail: gavin [at] stelfoxuk.com

Starts ASAP& offering intial 6 months contract, with few of long term renewals. Paying top market rates available with the benefit of Switzerland's Tax haven.

Program according to specifications, analysis datasets, pooled datasets, listings, and figures across several trials with a given compound and regulatory submission activities. Develop and comply with project/study programming standards and specifications following internal guidelines. Provide programming specifications for analysis datasets, pooled datasets and deliverables in consultation with the statistician. Support quality control and quality audit of deliverables Provide input as required at all meetings, discussions and activities covering aspects of Statistical Reporting on trial level activities Maintain efficient interfaces with internal and external customers and communicate effectively across line functions.

KEY JOB SKILLS

Experience using SAS in the analysis and the reporting of pharmaceutical data
Experience in Oncology therapeutic area
Working knowledge of database design/structures
Expertise with SAS (including SAS macro language)

DESIRABLE SKILLS

Advanced macro knowledge
Experience of complex programming Architecture or Application development

KEY BEHAVIOURS

Good team player
Good organizational
Continuous improvement mentality and attention to detail
Fluent English (oral and written)

URL: www.datashaping.com/jobs17173e.shtml
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Senior SAS Programmer / Team Leader - PRA International (Raleigh, NC)

2008-04-20T21:32:00.000-07:00

Job Description

We are currently seeking experienced Statistical SAS® Programmers for our growing Analysis & Reporting teams in the following offices: Raleigh, NC (World Headquarters); Lenexa, KS (Kansas City suburb). Several levels are available -- including Team Leader positions. The Analysis Programmer provides statistical programming support and validation of statistical analyses, datasets, tables, figures and listings. This person also provides statistical output for clinical study reports. The SAS Programmer will review clinical study protocols and case report forms, work with biostatisticians, writers and clinical staff to generate data summarization, analysis and reports; write and document programs; write command files; generate analysis databases in SAS; produce tables, listings and plots presenting data; review reports for consistency between text and tables; and perform ad hoc programming. As a Team Leader (Principal SAS Programmer), you will provide senior-level statistical programming support and validation of statistical analyses, datasets, tables, figures and listings. You will also serve as the Project Team Leader overseeing operational activities of the other Analysis Programmers. You will certainly have the opportunity to keep your technical programming skills sharp with hands-on work. However, you will also participate in the Analysis & Reporting team's implementation/testing of new software applications, the review and update of SOPs, and leading new business initiatives.

Qualifications

All candidates must possess a Bachelors degree -- however, an advanced degree (M.S. or Ph.D.) is preferred. As a successful candidate, you will possess a minimum of 2 years (SAS Programmer) or 5 years (Team Leader) SAS Programming work in a pharmaceutical company or CRO. Additionally, Team Leaders must have the demonstrated ability to plan, supervise, implement, and monitor the Statistical SAS Programming processes for multiple clinical trials.

Organization

PRA International provides employees the opportunity to work on complex, global trials that can change the course of medicine. For over 25 years, we have had a single mission - to become the best CRO in the drug development industry. Strategically aligned with leading pharmaceutical and biopharmaceutical companies worldwide, we provide clinical trial services and work on some of the most advanced drugs and biologics in development today .In addition to a unique professional challenge, PRA offers a pay-for-performance compensation philosophy, a commitment to professional development, and a culture that encourages work/life balance.

PRA International also offers:

Extended personal time off because we know you have a life outside of work
Competitive benefits plan
Flexible work schedules
Access to world-class therapeutic expertise unrivaled by any other CRO

URL: www.prainternational.com/careers.htm
Email: WaerhouseAimee [at] praintl.com

URL: www.datashaping.com/jobs17237d.shtml
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Biostatistican/SAS Programmer - Datatech (UK or France)

2008-04-20T21:31:00.000-07:00

Datatech have the following position. An exciting opportunity that could be just for you...

Are you a Biostatistician/SAS Programmer? Would you like to join a dynamic organisation with a flexible working policy?

Our client an international full service CRO is currently looking for a SAS Programmer or Statistician to join them to assist with the following responsibilities:

Review and update SOP’s
Statistical point of contact for allocated studies
Data presentations for inclusion in Clinical study Reports including production of such reports.
Statistical support during study design and set up
Development and review of Statistical Analysis Plans
Perform and oversee technical data management tasks

Suitable candidates must have at least 2 years experience gained within a CRO or Pharma company, have good knowledge of ICH-GCP and be a science graduate.

You will also need to be able to demonstrate a good understanding of clinical data, attention to detail, analytical and problem solving skills and good communication skills.

You must also be able to demonstrate professionalism, the ability to prioritise and manage tasks within a flexible environment and have sound knowledge of data management programming software.

For more information for this great opportunity, or to apply, please contact us at admin@datatech.org.uk.

URL: www.datashaping.com/jobs17165d.shtml
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Project Analyst - My InnerView Inc. (Wausau, WI)

2008-03-31T21:22:00.001-07:00

Departments(s): Research and Information Services

Job Summary

The Project Analyst works independently and applies standard methods to the collection and analysis of data by scheduling, collecting, verifying and analyzing data. The Project Analyst role is accomplished through database extractions and reporting software to produce client satisfaction survey reports as well as ad hoc reports.

Summary of essential job functions

Maintain longitudinal databases for satisfaction surveys and quality assurance
Assist in the compilation of parts of major project reports and/or to compile reports for projects, analyze computer or other output; working with other staff; reviewing data for accuracy and completeness.
Create visual presentations that depict the data collected and analyzed to clarify project information described in reports and presentations by constructing tables, charts and graphs; explaining data in an understandable manner.
Ensure the timely and accurate presentation of project information.
Document purpose, methods, techniques, conclusions, and implementation of major projects.
Research and evaluate problem reports and requests to resolve specific project data and information issues by analyzing problems; identifying the impact of problems or requests; and recommending solutions.
Participate in project meetings to inform others by presenting information; providing documents; drafting and editing reports, letters, and other written materials.
Work independently yet function as part of a team sufficient to accomplish project objectives.
Analyze data sufficient to verify and identify problems such as inaccurate and incomplete data and suggest solutions.

Minimum requirements

Bachelor degree in mathematics, computer science or related field. 2+ years experience in database management and report development.

Abilities required

Advanced knowledge of SAS
Advanced knowledge of Microsoft products including Word, Excel, Access, and PowerPoint
Comfort with large scale datasets as well as experienced at data importing and exporting between other software and SAS
Strong database knowledge preferred. Proficient with MySQL database, SQL language and database manipulations.

Physical and sensory requirements

Includes mobility, reaching, bending, lifting, grasping, fine hand coordination, ability to talk and hear, ability to read and write, ability to communicate with personnel and customers, ability to remain calm under stress. Ability to communicate effectively with staff.

Contact: Eric [at] myinnerview.com

URL: www.datashaping.com/jobs17151x.shtml
Please mention datashaping.com when applying. Thank you.

Data Analyst - My InnerView Inc. (Wausau, WI)

2008-03-31T21:20:00.000-07:00

Departments(s): Research and Information Services

Job Summary

The Data Analyst works with MIV staff to analyze data, maintain tables, perform analytical requests (meta-analysis). Role will include scheduling, collecting, verifying and analyzing data, as well as documentation of tables and the development of standard queries. The Data Analyst will perform database extractions and utilize reporting software to produce client satisfaction survey reports as well as ad hoc reports.

This position is based in Wausau, WI

Summary of essential job functions

Maintain longitudinal databases for satisfaction surveys and quality assurance
Assist in the compilation of parts of major project reports and/or to compile reports for projects, analyze computer or other output; working with other staff; reviewing data for accuracy and completeness.
Ensure the timely and accurate presentation of project information.
Maintain and document tables.
Create and maintain standardized queries for secondary data analysis.
Analyze data sufficient to verify and identify problems such as inaccurate and incomplete data and suggest solutions.
Work independently yet function as part of a team sufficient to accomplish project objectives.

Minimum requirements

Bachelor degree in mathematics, computer science or related field. 2+ years experience in database management and report development.

Abilities required

Intermediate to advanced knowledge of SAS
Advanced knowledge of Microsoft products including Word, Excel, Access, and PowerPoint
Proficiency in MS-Office graphics, macro development, visual basic.
Comfort with large scale datasets as well as experienced at data importing and exporting between other software and SAS
Strong database knowledge preferred; specifically, proficiency in SQL language, MySQL, and database manipulations.
Ability to write and communicate clearly in English. Proficiency in preparation of written reports, documentation and materials.

Physical and sensory requirements

Contact: Eric [at] myinnerview.com

URL: www.datashaping.com/jobs17152x.shtml Please mention datashaping.com when applying. Thank you.

SAS BI Systems Developer (London, UK)

2008-03-27T12:15:00.001-07:00

Use Your SAS-SY SAS Business Intelligence! - Please quote Reference Number AS / 9985 / DJ and Job Title in the Subject Line

Job Purpose:

As a SAS Business Intelligence Developer you will be using your strong SAS programming skills (SAS Base, SAS Macro and SAS Stat) to create reporting solutions that provide management with business critical information in order for them to make strategic decisions. You will also be creating the SAS engine that will automate analytical tasks such as customer profiling and segmentation.
Work will involve designing the user “front end” through to the back end detailed SAS reports using your strong interpersonal skills to obtain the enthusiasm of key stake holders for your design.
At the senior level you will be leading the team and taking overall responsibility for project development and success. As well as undertaking some international travel to ensure the successful international roll-out of the systems

Salary:

Excellent salary range from 30K 70K + Car + Bens. For the senior level salary candidates will have to demonstrate excellent technical and people management knowledge / experience.

Company:

You will be working for an employer of choice, a well established but rapidly growing international management consultancy firm with a strong foothold in the analytics, data management and data manipulation market. Excellent “go get” yet social culture.

Job Environment:

You will be working alongside other “work-hard, play-harder” enthusiastic and talented individuals that you can learn from and bounce ideas off of. The department’s overall purpose is the processing and manipulation of very large data sets in support of statistical analysis in order to provide customer insight that will in turn lead to robust database marketing campaigns

Your background and skills:

Probably you started life as a statistical analyst or econometrician but have in recent time focussed more on the IT side of things insofar as you have been creating the SAS data solutions that manipulate and present statistical data. Alternatively you may have a Business Information Systems or Informatics degree and have has a career in business intelligence of management information systems development.

Either way you will additionally have the following:-

Strong SAS programming skills
Experience of SAS Base, SAS Macro and SAS Stat
Good knowledge of SQL and /or VBA / VB Script
Knowledge of SAS for data manipulation rather than systems support
Good Excel
Ability to create a data plan and data flow diagram
Senior candidates need to demonstrate prior project and team leadership
Desirable: previous statistical modelling. Segmentation or customer profiling experience

Location: All Areas Salary/Rate: From £21-45K depending upon location and industry. Start Date: ASAP URGENT!

To apply or for more information: Call and / or send your CV to: sarah@corporate-recruiter.co.uk Please quote ref: AS/ 9985 / DJ in the subject line. Visit us at: http://www.corporate-recruiter.co.uk/JobSearch.aspx for more statistical jobs.

URL: www.datashaping.com/jobs17073f.shtml Please mention datashaping.com when applying. Thank you.

SAS Consultant, contract - VLS Systems (Summit, NJ)

2008-03-27T12:14:00.001-07:00

Requirement - 15868NJ Contact Name: Roy Sreedhar (roy@vls-systems.com) Location: Summit NJ Duration: 6 months Required Skills:

SAS macro language,SAS Business Intelligence Platform,PROC SQL
Level 2 - 4+ years of exp
Base SAS (including data step programming and DATA _NULL_)
SAS macro language
PROC TEMPLATE
PROC SQL
SAS/GRAPH
SAS Business Intelligence Platform (metadata server)
SAS/STAT (nice to have)

Assignment Description:

Analyzes (i.e., evaluates client area requirements and processes) and programs (i.e., prepares application system specifications).
Researches and evaluates alternative solutions and recommends the most efficient and cost effective solution for the systems design.
Incumbents in these positions do both systems analysis and coding.

URL: www.datashaping.com/jobs17074f.shtml Please mention datashaping.com when applying. Thank you.

SAS Statistician, contract (Toulouse, France)

2008-03-27T12:12:00.000-07:00

If this position is of interest to you please forward an updated CV to Kien-Sen.Lee [at] hayspharma.com, for a private consultation contact me (Kien-Sen Lee) directly on +44 207 922 7126.

Our client is based in the South of France and are actively seeking a Biostatistician for a 9 month contract initially, with opportunities to extend and rates depending on experience.

They are looking for candidates who are able to start ASAP and have experience in the Pharmaceutical industry.

DUTIES

Write detailed statistical analysis plans for clinical trials as well as for integrated summaries of efficacy and safety.
Analyse clinical trial data producing accurate results representing the outcome of the trial.
Validate statistical output.
Accurately interpret and clearly communicate statistical results and concepts to non-statisticians.
Co-author final integrated reports of clinical trial data writing thorough and clear statistical methods sections and producing the statistical appendix for the reports.
Provide statistical output as required for manuscripts and ensure that the results are accurately interpreted in the publications.
Provide input into statistical SOPs and general standardization efforts within the department (e.g. statistical methodology standards, standard data presentations).
Participate in interactions with regulatory agencies as required.
Collaborate effectively with members of clinical trial implementation teams and with Biometrics colleagues.

QUALIFICATIONS

Language and Education
Fluency in English.
Ph.D. or MSc in Statistics or Biostatistics or equivalent, with extensive and broad pharmaceutical/ biotechnology -experience.
Professional Skills and Experience
Working SAS knowledge and proficient in SAS statistical procedures.
Knowledge of ICH statistical regulatory requirements.
Personal Qualifications
Interpersonal skills, initiative, creativity.
Excellent communication skills.

Ian Kien-Sen Lee Consultant, Biostatistics - Hays Pharma

Hays Pharma is part of the Hays Plc group of companies - for all our latest jobs and industry news go to www.hayspharma.com.

www.smith-nephew.com Trevor Mole PhD Statistics Manager Smith & Nephew Wound Management Division

URL: www.datashaping.com/jobs17123e.shtml Please mention datashaping.com when applying. Thank you.

Statistician/SAS Programmer/Biostatistician - Verna Scientific (Bridgewater, NJ)

2008-03-27T12:10:00.000-07:00

contact: bob.harold [at] vernascientific.com Statistician - III (Senior) Verna Scientific Upper Gwynedd, PA

Statistical Programmer Verna scientific Jersey City, NJ

Sr. Statistician Verna Scientific Rochester, NY

Biostatistician Verna Scientific $2,000 Referral Reward* Bridgewater, NJ

All Open Positions at Verna Scientific Verna Scientific Seattle, WA (CA, PA)

URL: www.datashaping.com/jobs17072e.shtml Please mention datashaping.com when applying. Thank you.

Lead SAS Programmer - Genzyme Corporation (Cambridge, MA)

2008-03-27T12:07:00.001-07:00

Salary: 90-120/hour Industry: Clinical Trials Job Description

Currently, we are looking to staff (2) SAS Programming roles that require at least 7 years of experience which includes prior submissions experience.

There is a $2,000.00 referral bonus for every referral that we can place here at Genzyme.
We pay the bonus after the referral candidate is hired and has successfully completed 90 days with Randstad/Genzyme.

Job Description:

Submissions SAS Programmer-

Provide submission preparation and QC support for dataset section of submissions. QC datasets, documentation, programs, etc. to ensure submission readiness. Track all variables to source/origin and ensure documented clearly either on annotated CRF, external data documentation, or analysis dataset documentation. Ensure algorithms of derived variables adequately described in dataset documentation. Provide publishing support for preparation of define PDF files. Provide QC of draft published dataset content to ensure submission readiness. Provides support to Manager of Clinical Data Services and work with project team statisticians and SAS Programmers on the submission preparation of content for dataset section of submissions across many products. This is a contract role through Randstad and we will only consider consultants who are willing to work on a W-2 basis through Randstad. The hourly pay rate range is largely based on experience but the rate range is 90-120/hour. We do not relocated any candidates and do not sponsor visas.
Requires high (principal or senior) level SAS programming skills and good understanding of regulatory requirements for datasets for submission.
Certification in SAS is highly desired. Needs to be detail and quality oriented. Good communication skills necessary. Familiarity with publishing tools such as Adobe Acrobat a plus. Works under the oversight of the Manager of Clinical Data Services.

If you know of anyone looking for a new challenge that fits the job description above, please let me know and as always, I appreciate your referrals. I wish you continued success in 2008.

Qualifications

Requires high (principal or senior) level SAS programming skills and good understanding of regulatory requirements for datasets for submission.

Certification in SAS is highly desired. Needs to be detail and quality oriented. Good communication skills necessary. Familiarity with publishing tools such as Adobe Acrobat a plus. Works under the oversight of the Manager of Clinical Data Services.

Organization

Reports into the BioMedical Operations organization and specifically, the Statistical Programming team. www.genzyme.com Contact: kathleen.mcteague [at] genzyme.com Company: Randstad at Genzyme

URL: www.datashaping.com/jobs17067e.shtml Please mention datashaping.com when applying. Thank you.

SAS Analyst / Biostatistician (Toronto, Canada)

2008-03-27T12:05:00.000-07:00

Description: Sunnybrook Research Institute (SRI) is a hospital-based research institute in Toronto that is dedicated to the advancement of medical science. Scientists in the discipline of clinical epidemiology explore the causes, consequences and treatment of disease to improve patient care and ensure limited health care resources are used wisely. We are seeking a full time SAS Analyst/Biostatistician for a 15 month contract to work collaboratively with researchers, applying research methodology in the context of health services administrative data. As a member of our team of programmers and biostatisticians, you will:. Qualifications

Develop study designs
Assemble meaningful datasets for research questions
Conduct exploratory and statistical analyses of the data
Interpret the results
Produce reports
Participate in writing papers for peer-reviewed journals
Attend courses and training to maintain and expand professional skills
Organization

Qualified candidates are invited to submit their resume by March 21st quoting file # GD 3.08 to: Gale Delaney, Program Coordinator, Clinical Epidemiology Sunnybrook Health Sciences Centre 2075 Bayview Avenue, G1 06 Toronto, ON M4N 3M5 E-mail: resumes@ices.on.ca

We thank all applicants for their interest; however, only those invited for an interview will be contacted URL: www.datashaping.com/jobs17066e.shtml Please mention datashaping.com when applying. Thank you.

SAS Programmers Wanted - Acumen (Burlingame, CA)

2008-03-27T12:02:00.000-07:00

Acumen, LLC, together with its affiliated non-profit firm The SPHERE Institute, are seeking Quantitative Research Analyst/SAS Programmers to support research and consulting in the areas of health and social policy.

Position Description

This position will provide analysis on major federal and state issues such as:
Identifying strategies for pay-for-performance in public health insurance
Promoting data-driven decision-making in youth development and K-12 education
Monitoring health care claims to detect side effects from vaccines and prescription drugs
Ensuring the effective delivery of the new Medicare prescription drug plan, including
The accuracy of drug prices
Subsidies for low-income individuals
Drug utilization and costs across regions
Reducing risk of harm for individuals with developmental disabilities
Improving the information available to social workers in the child welfare system
Assessing the cost-effectiveness of alternative strategies for AIDS prevention and treatment in the US
Determining appropriate child care subsidy rates for low-income families

Acumen is a meritocracy where the level of responsibility is commensurate to one's demonstrated abilities and initiative; there is no bureaucracy or rigid job definitions to impede professional development. Research Analysts typically:

Interact with project officers and other government agency representatives and clients to access data and program information, determine analytical strategy and present findings
Develop research files from large confidential datasets, such as health care claims, school records, child welfare case management data, probation cases, and developmental disabilities client records, as well as in-house surveys
Conduct statistical and econometric analyses of data using statistical software
Work with senior researchers on analysis and evaluation

Qualifications

BA/BS in economics, statistics, math, public policy or related field is required; master's degree is preferred
Experience in quantitative analysis and proven analytical ability
Excellent SAS and/or Stata programming skills
Enthusiasm for learning

This is a full time position, with salary based on experience / education. Benefits provided. Apply by sending a cover letter and resume to jobs@acumenllc.com

URL: www.datashaping.com/jobs17121d.shtml Please mention datashaping.com when applying. Thank you.

Sr.SAS Programmer, contract - VLS Systems (Madison, WI)

2008-03-27T12:01:00.000-07:00

Req. ID: 15996WI Position Title: Sr.SAS Programmer Contact Name: Matt Daspet (matt@vls-systems.com) Location: Madison WI Duration: 6+ Months Required Skills: SAS experience with SAS verions 8 and 9

Job Description:

This candidate needs to be a strong SAS Programmer/Analyst with very good communication skills. They will have interactions with Executives and Directors. Candidate would have at least 5 years SAS experience with SAS verions 8 and 9. Could start tomorrow if they found someone. Will interview immediately. URL: www.datashaping.com/jobs17083c.shtml Please mention datashaping.com when applying. Thank you.

SAS programmmer - US Census Bureau (Washington, DC)

2008-03-27T11:58:00.000-07:00

US Census Bureau, the world's largest user of SAS products, has an immediate opening for a programmmer in its Data Management Division in the suburban Washington DC area.

The task involves data modeling, SAS DI Studio and other SAS/BI products, and technical writing. Both current Federal employees or those currently outside government will be considered.

Contact: jay.wind [at] ATT.NET

URL: www.datashaping.com/jobs17092c.shtml Please mention datashaping.com when applying. Thank you.

Statistics, SAS and Data Management (London, UK)

2008-03-27T11:55:00.001-07:00

One of the most exciting companies in London is currently looking for Statisticians, SAS Programmers and Data Managers for a range of positions within their modern West London site. This market research company has seen consistent and impressive growth since it's beginnings in the late 1980's and offers excellent career progression enabling you to develop your career in the direction that you want - be it moving your career internationally or developing skills in new areas. With a highly rated working environment and benefits package, this is a company with a lot to offer both in terms of your future career and your everyday professional life.

With opportunities at various levels for Statisticians, SAS Programmers and Data Managers with experience working in a statistical/database orientated industry or position (such as pharmaceutical, finance or retail) you will be working with key blue-chip companies on understanding data, data leveraging and providing solutions to meet their market needs.

Please contact James Brough in the Data Services team at i3 Pharma Resourcing if you are interested in either finding out further information, having a confidential chat or submitting your details for these great opportunities.

Email: james.brough [at] i3pharmaresourcing.com

URL: www.datashaping.com/jobs17143a.shtml Please mention datashaping.com when applying. Thank you.

OC/SAS Programming & Statistics (Berkshire, UK)

2008-03-02T17:24:00.000-08:00

We have 4 new jobs in Programming and Statistics with a pharmaceutical company based in Berkshire. Our client is a research driven group of companies responsible for a broad spectrum of innovative solutions to the marketplace- that ultimately improves quality of life. A privately owned company with a fantastic reputation, not only for its innovative products, but also voted in the top 100 companies to work for the 4th year running. This really is a company where you will be valued as an individual. Benefits include flexi-time, excellent pension and Health Care Scheme, subsidised canteen, as well as excellent training and development.

SAS Programmer Status: Perm Salary: up to £40k- £50k PA Details: If you are an experienced Programmer with some experience of SAS programming, then this may be ideal for you. Working in a small group you will coordinate the programming aspects of assigned clinical trials and to develop programs and tools for the management, reporting and analysis of clinical trial data. Additionally, with experience represent the Programming and Technical Support team on international teams and working groups.

Contract SAS Programmer Duration: 6 months Rate: £45-£55/hour Details: Working in a small group you will coordinate the programming aspects of assigned clinical trials and to develop programs and tools for the management, reporting and analysis of clinical trial data. Additionally, with experience represent the Programming and Technical Support team on international teams and working groups.

Contract OC Programmer Duration: 8 months (maternity cover) Rate: £45-£55/hour Details: In this role you will design & set-up databases in Oracle Clinical (O*C) and Remote Data Capture (RDC) for clinical trials, and to provide technical support for computerised systems / applications used by Biometrics and Data Management.

STATISTICIAN Status: Perm Salary: up to £49k PA (very competitive) Details: Working with a small group of Statisticians (~8) you will provide a comprehensive statistical service for the Company and be responsible for all statistical aspects of the clinical trials to which they have been allocated. In this role you will be working across different phases and therapeutic areas. Limited programming duties, as there are a team of onsite programmers. Excellent opportunities for training and development.

About CK Clinical

CK Clinical is a privately owned recruitment company, formed in 2004 to provide a professional and efficient recruitment service to the pharmaceutical, biotechnology and contract research industries. Since our formation we have enjoyed sustained growth and are a proven, established and valued recruitment partner in our chosen sectors. CK Clinical are preferred supplier to the top 5 global organisations within our sector as well as having agreements in place with smaller, more niche organisations too.

We know finding a new job can be a rather daunting process, whether you are an expert in your field or a new graduate ,CK Clinical are here to help you at every step of the process. We can offer expert advice on CV writing, interview tips and techniques, or simply just help you gather all the information you may need. We aim to put you first, be supportive and make finding your ideal job a pleasurable experience.

Contact: SBrunnen [at] CKCLINICAL.CO.UK

URL: www.datashaping.com/jobs17050e.shtml Please mention datashaping.com when applying. Thank you.