What are the responsibilities and job description for the Clinical Programmer position at GForce Life Sciences?
Consultant, Clinical Programmer, Pharmaceutical
Our client, a global pharmaceutical organization, has engaged GForce Life Sciences to provide them with a Clinical Programmer. In this role, you will be responsible for assigned statistical programming activities on a collaboration and license agreement for Europe, China, and other territories.
This SAS programmer will support an ongoing and planned clinical trial analysis, reporting, and MAA submission. The successful candidate will be well-versed in SAS programming, knowledgeable in CDISC data standards, and someone who enjoys collaborating with multiple departments.
Summary
Our client, a global pharmaceutical organization, has engaged GForce Life Sciences to provide them with a Clinical Programmer. In this role, you will be responsible for
Responsibilities:
- Independently develop/validate programs that generate SDTM and analysis datasets based on ADaM specifications
- Prepare/QC ADaM datasets documentation: Define.xml, Reviewer’s Guide, and analysis metadata report
- Independently develop/validate programs that generate tables and listings specified in the protocol or the Statistical Analysis Plan (SAP)
- Perform quality control on final reports
- Provide QC and validation reports
- Support the development of technical programming specifications for ADaM standards
- Communicate with programming and statistics leads, data managers, and other team members
- Provide project progress updates of programming activities
Qualifications/Experience:
- BS/MS in Statistics, Biostatistics, Computer Science, Mathematics or Life Sciences
- 10 years of statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry
Required Skills Include:
- Strong SAS programming skills required in Windows & UNIX environments with proficiency in SAS/Base, SAS Macros, SAS/Stat
- Knowledge of working in SAS Grid environment with experience in SAS Enterprise Guide and SAS Studio is a plus
- Experience with all clinical phases I, II, III, and IV of trials is desirable
- Good understanding of standards specific to clinical trials such as CDISC, SDTM, ADaM, MedDRA, WHODRUG
Term & Start
- 12-month contract with potential to extend
- Remote – Must be able to work in EST hours
- 2-3 Video Interviews – 2 weeks to start from an offer
- Health benefits available (medical, dental, vision)
