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Senior Manager, Biostatistics
5-7 years
Hyderabad / Secunderabad
1 vacancy
Senior Manager, Biostatistics
Bristol-Myers Squibb
posted 5d ago
Job Role Insights
Flexible timing
Key skills for the job
Job Description
- Collaborate s in design of clinical study including methodology , data analysis & interpretation, and reporting of study results.
- Author s and/ or review s protocol synopsis, protocol, statistical analysis plans, case-report forms, clinical study reports, associated publications, and other study level specification documents with minimum supervision
- Perform s and/or validate s statistical analyses, advise ways to maximize clarity of data display
- Communicate s results to cross-functional teams, provide s data interpretation in study documents such as clinical study reports, and publications.
- Translate s 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 develop s technical knowledge of statistical methodology and how it is appropriately applied in trial design and data analysis for clear, concise, high-quality results.
- Continually enhance s knowledge of drug development process, regulatory and commercial requirement
- Develop s & advise s team members.
- Effectively communicate s the GBDS Mission and Vision in a fashion that generates pride, excitement and commitment within GBDS.
- Enable s 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 P hD 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 learn regulatory requirements & clinical trial design, data analysis and interpretation, work successfully within cross-functional teams, organize multiple work assignments and establish priorities
- 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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Anonymous · Technology / IT
in Hyderabad / Secunderabad, Telangana
Inclusive work culture, work on latest technology stack, good leave policies, average hikes.
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