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106 Bristol-Myers Squibb Jobs
Senior Manager, Biostatistics - Clinical Pharmacology
2-7 years
Hyderabad / Secunderabad
1 vacancy
Senior Manager, Biostatistics - Clinical Pharmacology
Bristol-Myers Squibb
posted 1d ago
Job Role Insights
Flexible timing
Key skills for the job
Job Description
- Collaborates in design of clinical study including methodology, data analysis interpretation, and reporting of study results.
- Authors and/or reviews protocol synopsis, protocol, statistical analysis plans, case-report forms, clinical study reports, associated publications, and other study level specification documents with minimum supervision
- Performs and/or validates statistical analyses, advise ways to maximize clarity of data display
- Communicates results to cross-functional teams, provides data interpretation in study documents such as clinical study reports, and publications.
- Translates scientific questions into statistical terms and statistical concepts into layman terms.
- Compliant with BMS processes and SOPs, adherence to global and project standards within an indication or therapeutic area and responsible for quality of deliverable.
- Continually develops technical knowledge of statistical methodology and how it is appropriately applied in trial design and data analysis for clear, concise, high-quality results.
- Continually enhances knowledge of drug development process, regulatory and commercial requirement
- Develops advises team members.
- Effectively communicates the GBDS Mission and Vision in a fashion that generates pride, excitement and commitment within GBDS.
- Enables a culture of inclusiveness, respect for diversity, compliance with process and allows for the questioning and challenging of others in a respectful and constructive manner.
- Fresh PhD with 3+ years experience or MS with 5+ years experience in statistics or biostatistics or related scientific field with clinical trials, drug development, pharmaceutical industry or healthcare experience
- Proficiency in scientific computing/programming (SAS, R or Python) and implementation of advanced statistical analysis, data manipulation, graphing simulation.
- Good interpersonal, communication, writing and organizational skills
- Ability to:
- Experience in standard and advanced statistical methods is preferred.
- Good understanding of regulatory requirements clinical trial design is preferred
Employment Type: Full Time, Permanent
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