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Senior Biostatistics Operations Lead

2 months ago

Berkeley Heights, New Jersey, United States Bristol-Myers Squibb Full time
About the Role

We are seeking a highly skilled Senior Biostatistics Operations Lead to join our team at Bristol-Myers Squibb. As a key member of our GBDS TA Operations team, you will play a critical role in managing resources and budgets for biostatistics and programming deliverables.

Key Responsibilities
  • Support the Biostatistics TA Head in managing resources and budgets for biostatistics and programming deliverables within the TA.
  • Drive consistency and excellence in developing strategic plans for GBDS deliverables in support of portfolio priorities within the TA.
  • Collaborate with Biostatistics TA Head and Programming TA Head by providing accurate portfolio and resource data to ensure timely resource planning.
  • Partner with the Biostatistics TA Head to provide strategic thought partnership towards sourcing options within a TA balancing priorities, risks, speed, quality, and cost.
  • Collaborate with Biostatistics TA Head to ensure key priorities are escalated for awareness and discussed with TA leaders through TA LT meetings and Town Halls.
  • Validate and provide consolidated information on the health of the GBDS TA to the Biostatistics TA Head and Programming TA Head.
  • Leverage matrix management with the Bus Ops Team to bring awareness and recommendations relating to key initiatives at the GBDS and GDD levels that may impact TA strategic priorities.
  • Monitor financial aspects of doing business with our vendors and proactively monitor risk associated with budgets.
Success Factors
  • Ability to effectively demonstrate fully functioning capability in the following areas:
  • BMS Core Values: Passion, Innovation, Urgency, Accountability, Inclusion, and Integrity.
Requirements
  • Graduate degree and/or relevant experience in statistics, computer science, or other related discipline.
  • At least 9 years of Pharmaceutical/R&D or other related experience in a regulated environment.
  • Experience working at the strategic level and when to delve deeper to resolve issues and challenges.
  • Extensive experience managing multiple, complex vendor relationships on clinical trial related activities.
  • Superior project management skills/experience with proven ability to manage timelines and resources across large teams/projects.
  • General knowledge of regulatory submissions and/or other regulated activities (Market Access, Annual Reporting, Clinical Trial Transparency).
What We Offer

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.

We are committed to creating a diverse and inclusive work environment that fosters collaboration, innovation, and growth. If you are a motivated and experienced professional looking for a new challenge, we encourage you to apply for this exciting opportunity.