Saama Technologies is a leader in AI-driven clinical data analytics, helping pharmaceutical and life sciences companies accelerate drug development and commercialization. With cutting-edge Artificial Intelligence (AI), Generative AI, and advanced analytics, Saama automates critical clinical processes, ensuring faster time-to-market. Explore more at saama.com.
Job Description
Key Responsibilities:
- Work independently on SDTM and client-specific mappings for clinical trial data.
- Develop and validate CDISC-compliant (SDTM, ADaM) datasets for regulatory submissions.
- Utilize SAS, Python, or R programming to process and analyze clinical data.
- Identify and troubleshoot data issues, ensuring high-quality deliverables.
- Assist in CRF annotations, data consistency checks, and debugging SAS macros.
- Collaborate with Biostatistics, Data Management, and Programming teams.
- Follow client SOPs and compliance guidelines for clinical data submissions.
Skills & Qualifications:
✔ 2-4 years of experience in Statistical Programming (Clinical/Pharma domain).
✔ Strong knowledge of CDISC standards (SDTM, ADaM) and regulatory submissions.
✔ Proficiency in SAS programming (mandatory).
✔ Knowledge of Python/R programming (added advantage).
✔ Understanding of clinical trial data and domain knowledge.
✔ Excellent communication and teamwork skills.
Education:
- B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Computer Science, or related field
