Associate Director, Biostatistics

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients’ lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

Ph.D. in Statistics with 8+ years (or + years for MS) pharmaceutical experience as a statistician supporting clinical trials.

Responsibilities will include, but are not limited to, the following:

Actively provide statistical support to BMS Research and Development.
  • Serves as the global lead statistician in the support of trial Phases I-III of drug development for a therapeutic area.
  • Manages multiple studies within an indication or therapeutic area.
  • Serves as an advisor to statisticians assigned to the project to ensure high quality and timely deliverables.
  • Guides global staff in the preparation of Statistical Analysis Plans. Shepherds the plan through clinical review to ensure worldwide organizational acceptance of the statistical design, endpoints, and proposed analyses.
  • Ensures consistency and adherence to standards within a project.
  • Contributes to Clinical Development Plans, submissions and post-submission strategies, preparations and defense, ensuring quality and timing thereof.
  • Provides statistical support for Health Authority requests, publications, presentations, and posters at medical conferences/symposia, as assigned.
  • Contributes to, and provides training on new departmental statistical topics, SOPs, WPs.
  • Impacts directly on overall business and Biostatistics performance through the ability to influence and work in a consultative manner with senior stakeholders.
  • Sets project level priorities.
  • Manages resources to meet project team timelines.
  • Escalates issues to functional management as necessary.
  • Makes recommendations or resolves technical, quality, and timeline issues.
  • Manages outside CROs and contractors.
  • Recommends external statistical experts for consultation.
  • Provides guidance to employee's development plan and carries out performance review and feedback
  • Evaluates the effectiveness of Biostatistics programs, policies, and processes to meet evolving stakeholder needs
  • Leverages best practices in Biostatistics management to enhance efficiencies.
  • Provides directions to project teams using statistical expertise and project knowledge.
  • Manages team conflicts to resolution and improved team collaboration.
  • Maintains close collaboration and working relationships with stakeholders.
  • Manages conflicts with external partners/customers.
  • Represents Biostatistics function at cross-functional meetings.
  • Oversees/coordinates biostatistical activities on global submission teams.
  • Partners with senior line management to shape Biostatistics strategy in alignment with the business strategy.
  • Works closely with stakeholder leaders to develop and implement high impact business initiatives.
  • Leverages existing Biostatistics programs, policies, and procedures to create value-added solutions for Biostatistics.
  • Provides proactive expertise, coaching, and counseling to stakeholder leaders, employees, and peers on complex Biostatistics and stakeholder issues.
  • Provides leadership
  • Sought out thought leader, providing coaching and mentoring to peers, Statisticians/Programming team members and others
  • Provides continuous feedback to peers and leaders
  • Proactively seeks ways to gain broader experience/perspectives and focuses on a robust professional development plan
  • Leads cross-functional collaboration and conducts meetings to gain the trust and respect of members, make decisions on business issues and freely challenges and expresses opinions
  • May manage and or develop staff; provide coaching and mentoring, monitors other's performance, makes recommendations on resource allocations and provides feedback via formal/informal appraisals

Skills/Knowledge Required :
  • Ph.D. or MS in statistics (or related field) with a focus on statistical methods appropriate for clinical trials.
  • Experience in clinical drug development: 8+ years for Ph.D., 10+ years for MS. Experience in the relevant therapeutic areas is preferred.
  • Demonstrated skill in the planning, analysis and reporting of clinical trials.
  • Detailed knowledge of statistical methodologies, relevant therapeutic areas, and statistical regulatory requirements.
  • Previous experience in leading and completing a task force or supervising statisticians.
  • Abreast of clinical trial design concepts.
  • In-depth knowledge of all phases of the drug development process.
  • Demonstrated ability to work in a team environment with clinical team members.
  • Good interpersonal, communication, writing and organizational skills.
  • Abreast of statistical method development and able to decide on the optimal methods acceptable to regulatory agencies.
  • Abreast of relevant project area's clinical trial development and regulatory requirements.
  • Establishes performance standards and commits to evaluation and review of developmental opportunities.



Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

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