Bristol-Myers Squibb Company

Director Global Biometric Sciences

Princeton, NJ, US
Apr 13, 2018
Required Education
Position Type
Full time

Wallingford Transition

GBS Biostatistics Lead- Early Asset Development, Global Biometric Sciences


The GBS Biostatistics Lead is a member of the Early Asset Development team (EADT). Along with the clinical and regulatory leads, the GBS Lead is responsible to provide scientific and strategic leadership and has a shared responsibility for developing the clinical/regulatory strategy. Among other things, the GBS Lead provides strategic input into the design/planning of clinical trials, data analysis approaches, interpretation of findings and crafting of key messages. The GBS Lead typically represents GBS in meetings with global regulatory agencies. The GBS Lead has accountability for the performance of the GBS team and develops an effective partnership with the GBS Planning and Execution Lead to ensure the team's ability to execute with quality in agreed to timelines. The GBS Lead may have direct reports and is responsible for coaching and developing all members of their team. GBS Leads may serve as members of the GBS Extended Leadership Team and contribute to the continuous improvement of GBS, which includes but is not limited to recruitment of talent, improving processes and contributing to the strategic initiatives/directions of GBS.

Primary Responsibilities:

  • Member of an EADT. Contributes to all aspects of the development strategy. Partners with the team to prepare a development strategy that will enable the effective and safe utilization of the product.
  • Assumes a leadership role within the GBS organization by contributing and having influence in the development of GBS capabilities, talent management and sharing of best practices across GBS.
  • Effectively communicates the GBS Mission and Vision in a fashion that generates pride, excitement and commitment within GBS.
  • Invests in developing knowledge outside of traditional statistical expertise in the clinical, regulatory and commercial environments that impact the development team.
  • Oversees the selection of trial designs, endpoints, statistical analysis strategy, development of DMC proposals, and contributes to the interpretation of trial results and development of the key messages and their communication.
  • Together with the GBS Planning and Execution Lead, identifies project resource needs, and, in coordination with the development team, aligns team's approved objectives and timelines with the GBS project level book of work and the allocation of GBS resources to ensure effective delivery.
  • Has accountability for the GBS team (internal and/or external) to effectively deliver on both scientific accountabilities and operational tasks (e.g. tables, figures, listings), while maintaining compliance with global standards, SOPs and established work processes.
  • Effectively communicates with internal scientific governance bodies, clinical and regulatory partners, external opinion leaders and manages relationships and interactions with development alliance partners.
  • Builds the external reputation of BMS R&D via external interactions.
  • Presents or responds to questions at Global Regulatory Meetings
  • Manages the GBS project team to take advantage of opportunities, overcome obstacles, and achieve program milestones. Facilitates the development of innovative solutions to both broad development issues and statistical issues.
  • Contributes to GBS strategic initiatives through participation on initiative teams and/or contributing in feedback sessions.
  • Line/matrix management responsibilities:
    • Effectively manages, develops, evaluates and retains direct reports, resulting in an increasing level of capabilities for the GBS organization.
    • 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.
    • Conducts objective setting, mid-year reviews and end of year discussions in compliance with BMS policies.
    • Establishes a development plan with each direct report and meet as frequently as required to deliver timely positive/development feedback and coaching.
    • Ensures compliance of direct reports with training requirements and all relevant SOPs.
    • Differentially recognizes, develops and rewards talent in roles that are critical to BMS and GBS future growth through leadership opportunities and areas of visibility within and external to GBS.



The contributions of the GBS Lead directly enhance the quality of our clinical research and result in better decision making within R&D. Through this, BMS will be able to make early and quality decisions on its assets and ultimately have improved success rates for regulatory approvals and enhanced market acceptability. By managing stakeholder relationships, the effectiveness of the development team will be enhanced, with issues being resolved rapidly, resulting in more effective use of all the team's resources. GBS Leads will contribute to developing biostatisticians, P&E leads and programmers. They will influence and contribute to the strategic directions of GBS.

Success Factors:

Effectively demonstrates fully functioning capability in the follow areas:

BMS Core Behaviors:

• Passion

• Innovation

• Accountability

• Speed

GBS Leadership Success Factors:

o Leading and Managing Change

o Influence and Impact Relationships

o Decision Making

o Building a Learning Environment

o Emotional Intelligence

o Managing and Developing Performance

Note: Please refer to ancillary document for definitions and descriptions of aforementioned success factors





  • Statistical expertise, medical/clinical trials knowledge, and project management skills.
  • PhD degree in statistics or biostatistics or Master's degree with relevant experience in the Oncology Therapy Area preferred.
  • > 7 years of Pharmaceutical/R&D or other related experience in planning and managing statistical aspects of clinical development projects and clinical trials reporting to support regulatory filings.
  • Excellent verbal and written communications skills.
  • Strong interpersonal skills and demonstrated ability to develop relationships within the organization.
  • Demonstrated experience in designing and executing research activities in close collaboration with medical, clinical, regulatory and commercial partners.
  • Ability to work successfully in cross-functional teams leading to successful global regulatory filings and approvals.
  • Strong communication/presentation skills with ability to tailor the message to the key stakeholder for effective impact and influence.
  • Ability to be flexible and adapt quickly to the changing needs of the organization.
  • Ability to organize multiple work assignments and establish priorities.
  • Demonstrated ability to operate and lead in a matrix organization, building successful working relationships and effective stakeholder management in an environment with multiple lines of authority and competing needs.


Supervisory Responsibility:

Matrix and the potential to have direct management responsibilities.