Job Description
Key Responsibilities:
- Develop, validate, and maintain statistical programming codes for clinical trials.
- Generate SDTM, ADaM datasets, and TLFs (Tables, Listings, and Figures) as per CDISC standards.
- Perform quality control checks on statistical outputs.
- Collaborate with biostatisticians and clinical teams to ensure accurate data analysis.
- Ensure compliance with regulatory guidelines (ICH-GCP, FDA, EMA).
- Utilize Base SAS for data manipulation and reporting.
Eligibility Criteria:
- Educational Qualification:
- B.Tech/B.E (IT, Computer Science, Biotechnology, Bioinformatics)
- MCA/MSc (IT, Computer Science, Mathematics)
- B.Pharm/M.Pharm or Masters in Life Sciences (with 4+ years of education after 10+2)
- Mandatory: Base SAS certification/training.
- Year of Passing: 2023 or 2024 only.
About IQVIA
IQVIA is a global leader in clinical research, healthcare analytics, and commercial solutions for the life sciences industry. The company provides advanced data science, AI-driven insights, and clinical trial management to accelerate drug development and improve patient outcomes.
Why Join IQVIA?
✔ Global Exposure – Work with top pharmaceutical & biotech companies.
✔ Career Growth – Structured learning & development programs.
✔ Innovative Work Culture – Cutting-edge technology & data science projects.
✔ Competitive Salary & Benefits – Health insurance, performance bonuses, and more.
📍 Job Location: Kochi, Kerala
How to Apply?
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