Global Development Lead, Internal Medicine (Sr. Director)

Role Summary

The Global Development Lead (GDL) represents Clinical on the Global Medicine Team and is the single clinical point of accountability for clinical development for assigned Internal Medicine assets within Pfizer. The GDL leads the cross-functional Clinical Development Team in the design, execution, and interpretation of studies to support worldwide regulatory submissions and creates endorsement for the Clinical Development Plan and protocol documentation. They are a therapeutic-area subject matter expert in clinical drug development and may support other late-stage assets, trial design, execution, and reporting, and may partner with external companies as part of Pfizer’s Partner of Choice model.

Responsibilities

• Partners effectively with the Prod Team Lead to negotiate tradeoffs, milestones and ensure delivery of the clinical program in line with agreed timelines and budget.
• Responsible for comprehensive clinical development plan to secure approval and reimbursement globally (including China and Japan) along with creating the pediatric investigation plan / pediatric study plan and associated protocol design documents working closely with individual trial clinicians to ensure trial feasibility and optimized operational execution.
• Provides product/program specific input for target product profile(s).
• Willingness to bring innovative thinking and bold decision making across clinical development programs and individual studies.
• Develops specific clinical development enabling strategies including digital/ innovation and patient engagement approaches.
• Partners with Trial clinicians on governance reviews (incl Sci/Ops) for assigned clinical studies. Provides category clinical development strategy input and insights to trial clinicians for assigned clinical studies.
• Provides therapy area/indication expertise in support of clinical review of clinical data – including CRF design, assistance in signal interpretation, contextualizing adverse events as required.
• Provides specialized medical monitoring support for individual trial team, if required.
• Key partner in trial-level statistical analysis plan, table-listings-figures, database release in partnership with statistics and programming.
• Develops submission level deliverables (IAP, IARP and submission TLFs). Responsible for submission deliverables including SCE and SCS.
• Support appropriate interpretation and communication of clinical trial data.
• Review and approve submission level safety narrative plan.
• Supports product label development and maintenance.
• Engage key external stakeholders e.g., Ad boards, Steering Committees, DMC, Adjudication Committees, patients and patient advocates and other external stakeholders, to drive strategic insight generation to support clinical development strategy and PDD development.
• Provides regulatory submission support (DSUR, PBRER) submission disclosure deliverables and product defense.
• Ensures compliance with internal SOPs and external regulatory standards.
• Review IIR proposals.

Qualifications

• Basic Qualifications: BS with 12 yrs or PhD with 7 yrs, relevant clinical/industry experience.
• Experience:
  • Experience leading large cardiometabolic late-stage development programs.
  • Relevant experience and track record of success in academia and/or the biopharmaceutical industry in clinical research and development.
  • Extensive knowledge of clinical development, global and regional regulation, ICH/GCP, adverse event management.
  • Demonstrated clinical/medical, administrative, and project management capabilities, as well as effective verbal and written communication skills in relating to individuals both inside and outside Pfizer.
  • Demonstrated experience managing and training large teams in clinical development.
  • Demonstrated experience in designing and launching large teams (preferred).

Skills

• Medical / Scientific credibility / Excellence - Track record of achievement in pharmaceutical development, able to coordinate and execute clinical development or lifecycle strategy. Demonstrated understanding of the complexities and recent developments in the principal disease areas; confident discussing scientific / mechanistic aspects of drug development, also comfortable in discussing regulatory issues.
• Management experience - Able to work in a highly complex matrixed environment and able to influence cross-functional teams.
• Leadership - Persuasive and effective leader of staff.
• Influencing - Able to manage and motivate internal teams on clinical trials.
• Conflict Management - Able to act as mentor / coach to others to improve conflict management skills; steps up to conflicts, seeing them as opportunities; reads situations quickly; can hammer out tough agreements and settle disputes equitably; prepared to take responsibility for a decision made and support this, even though it may be unpopular.
• Team Building - Shares wins and success; fosters open dialogue; lets people finish and be responsible for their work; defines success in terms of the whole team; creates strong morale and spirit in his/her team; creates a feeling of belonging to the team.
• Accountability - Take personal responsibility for results, pushing self and others to exceed goals and deliver results.
• Change agile - Able to demonstrate perspective and poise in the face of uncertainty and effectively get things done amidst organizational change.
• Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.

Additional Requirements

• Up to 30% travel may be required.
• Relocation support available.
• Hybrid work arrangement: live within commuting distance and work on-site an average of 2.5 days per week.