Not specified; not specified; competitive benefits...
Hybrid (50% onsite)
Phd in statistics or biostatistics with 6+ years experience
Proficiency in sas, r, or python for advanced analysis
Expertise in clinical trials methodology and regulatory landscape
Bristol Myers Squibb is seeking an Associate Director of Biostatistics to contribute to clinical trial design, data analysis, and regulatory submissions. The role emphasizes collaboration within cross-functional teams and requires significant experience in biostatistics, clinical trials, and advanced statistical methodologies
Job Summary
The role involves contributing to trial design, protocol development, and preparation of regulatory submissions to transform patients' lives.
Candidates will lead high-risk, high-complexity projects requiring the development of new statistical methodologies and strategic input.
Bristol Myers Squibb offers a wide variety of competitive benefits and programs supporting work-life balance and career growth.
Matching Summary
Match Score: 85
Bristol Myers Squibb is seeking an Associate Director of Biostatistics to contribute to clinical trial design, data analysis, and regulatory submissions. The role emphasizes collaboration within cross-functional teams and requires significant experience in biostatistics, clinical trials, and advanced statistical methodologies.
Salary
Not specified; Not specified; Competitive benefits and programs offered
Skills & Requirements
Must-have
PhD in Statistics or Biostatistics with 6+ years experience
Proficiency in SAS, R, or Python for advanced analysis
Expertise in clinical trials methodology and regulatory landscape
Nice-to-have
Experience with cell therapy and novel problem-solving
Thought leadership through publications and advisory panels
Strong interpersonal and cross-functional collaboration skills
Key Requirements
PhD (6+ years) or MS (8+ years) in statistics/biostatistics
Clinical trials and drug development industry experience