Offer summary
Qualifications:
B.S. or equivalent in related field, 5 years clinical research programming experience, 3 years experience in pharmaceutical industry, Proficient in SAS and CDISC standards, Experience with MS Office Suite.Key responsabilities:
- Support programming for study deliverables
- Collaborate with Data Management and Biostatistics
- Create and validate SDTM and ADaM datasets
- Generate TFL output as per requirements
- Maintain supporting documentation