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Job Description
Key Responsibilities
- Lead statistical tasks for clinical trials, including protocol and statistical analysis plan (SAP) development, exploratory PK,PD analyses, biomarker studies, and regulatory reporting.
- Innovate trial designs, interpret complex results, and provide expertise for health authority submissions and cross-functional teams.
- Collaborate with clinical, regulatory, and R&D teams to ensure high-quality data analysis using R, SAS, or similar tools, while mentoring junior staff.
- PhD in Biostatistics, Statistics, or related field.
- 3-5 years in biostatistics roles at global pharmaceutical firms (e.g., Novartis, Pfizer, Roche), with proven expertise in clinical trial design, causal inference, and regulatory compliance.
- Strong programming skills in R,SAS, excellent communication for multidisciplinary teams, and familiarity with neuroscience or pharma drug development.
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- Experience with Bayesian methods, machine learning for biomarkers, or Phase I-III trials in neuro,pharma settings.
- Ability to represent the company at conferences and drive innovative statistical strategies.
Skills
Data AnalysisMachine LearningAnalyticsIf an employer asks you to pay any kind of fee, please notify us immediately. Jobaaj does not charge any fee from the applicants and we do not allow other companies also to do so.
Important dates & deadlines?
Application Deadline
05 Jun 26, 02:29 PM IST
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