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Job Details

Statistical Programmer

Company: CROMSOURCE
Location: United Kingdom
Reference: HQ00001094
Closing Date: 24 May 18
Type: Contract
Salary (£): On Application
Benefits: Excellent and Comprehensive Benefits – see below

Job Summary:

TalentSource Life Sciences is currently searching for an experienced Statistical Programmer Analyst, with excellent CDISC and project programming experience, to work with one of our partner pharmaceutical companies in Hertfordshire.       This is a freelance position with TalentSource for 6 months initially with the possibility of being extended, on a full time basis. This will be an office based position, with some flexibility to work from home after the first 3...

Requirements:

TalentSource Life Sciences is currently searching for an experienced Statistical Programmer Analyst, with excellent CDISC and project programming experience, to work with one of our partner pharmaceutical companies in Hertfordshire.

This is a freelance position with TalentSource for 6 months initially with the possibility of being extended, on a full time basis. This will be an office based position, with some flexibility to work from home after the first 3 months at the discretion of the line manager. The successful candidate will be working on studies dedicated to one client.

TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having the continuous support from your TalentSource Line Manager who will work closely with you to support your professional development and growth.

Job Purpose:

The Statistical Programmer provides statistical software programming solutions, documentation to Biostatistics, support analysis and reports for clinical trial and/or project data for regulatory submission. The Statistical Programmer will support the Project Programmer in designing and implementing the statistical programming strategy for the project. The Statistical Programmer coordinates and performs statistical programming activities with agreed objectives, standards, deadlines and other requirements with respect to the specifications, program development, quality assurance and report delivery that are attained in accordance with applicable processes.

Responsibilities:

· Provide advice and support to the statistical team on programming activities related to the analysis and reports of assigned drug development study/project results.

· To assess and clarify requirements, provide statistical programming solutions and ensure their efficient implementation.

· Contribute to Case Report Form (CRF) development and data structures definitions for clinical trials. Ensure consistency and adherence to available standards.

· Ensure that user acceptance testing on the structure and quality of data provided by Data Management is performed.

· Perform the user acceptance testing of data structure and execute data quality acceptance checks. Develop additional study-specific checks as required.

· Develop programming specifications to ensure consistency with the statistical specifications for analysis datasets (VADs), pooled datasets, listings, tables, and figures.

· Plan and perform programming, validation and documentation activities for VADs, pooled datasets, listings, tables, and figures according to specifications, with high quality and within agreed time lines.

· Adhere to statistical programming standards, effective use of available standard programs and compliance with Standard Operating Procedures.

· Support regulatory submission specific activities, e.g. electronic submission creation.

· Maintain efficient interfaces with internal and external customers.

Education / Qualifications:

· University education (BSc or MSc) or equivalent in Statistics, Computer Science, Mathematics or other analytical field.

· Strong previous statistical programming experience in Europe

· Experience with SAS programming language with SAS/Base, SAS Macro, SAS/Graph, SAS SQL and some SAS/STATS within a Clinical/Pharmaceutical environment

Experience, Skills, Knowledge:

· Good knowledge of drug development processes in particular on collection, storing, processing and analysis of clinical trial data

· Has well developed planning and analytical abilities

· Communicates clearly and effectively in written and oral form

· Fluent in English, written and oral

If you have the experience and are interested in discussing the role for this position, please contact Laura Guascone, Laura.Guascone@CROMSOURCE.com.

Why choose TalentSource Life Sciences/CROMSOURCE?

CROMSOURCE is a family owned international, full-service Contract Research Organization who, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. TalentSource Life Sciences is a fully dedicated flexible resourcing unit within CROMSOURCE and the successful growth has been achieved by putting high quality and client focus at the heart of everything we do.

Our employees are the most valuable company asset and we value resources and ensure they work in a friendly, family environment and develop their skills and talents. Human Resources is the fulcrum around which all activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel clear tools to manage both internal and client processes with the same methodology.

Our approach is to equally value our clients and our own people. We know that we are not simply providing 'staff' or 'resources'. We are providing expert people. Highly talented, well trained, motivated people who make a positive difference to the work of our clients every day. Together we help our clients succeed in their work developing medicines and medical devices for patients around the world. Our large management team consists of a people with an extended experience within pharma and a high level of market knowledge

CROMSOURCE comes from the merger of MSOURCE and CROM in 2011 and we are great at recruitment and staffing services! We're proud to partner with the industry's leading Pharmaceutical, Biotechnology, Medical Device and Marketing Communications worldwide, securing great global talent. We our open, friendly and approachable and aim to support you through the recruitment process every step of the way.

For the client client-facing positions, the successful candidates must be confident and be able to drive the role and themselves and to work autonomously in close liaison with a line manager at TalentSource, who will provide you with mentoring and guidance. Most of our roles are permanent positions with CROMSOURCE and you will be working on studies for just one client.

How can we help you on your next career move? Learn more on LinkedIn, YouTube, Facebook, Twitter, and Glassdoor.

Keywords: Statistical Programmer, Statistician, SAS, CDISC, Programmer, Data Management, SAS/Base, SAS Macro, SAS/Graph, SAS SQL, SAS/STATS Clinical, Pharmaceutical

Statistical Programmer, Statistician, Freelance

Apply for this job: Statistical Programmer

Contact Information:

Address:  UK Office
CROMSOURCE Suite 3 Lomond Court Castle Business Park Stirling United Kingdom
FK9 4TU
Scotland
Tel:  +44 (0) 1786 468990
Website:  Visit Our Web Site

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