Senior Director, Clinical Pharmacology

Vertex Pharmaceuticals Incorporated

$232K — $348K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D. or Pharm D in relevant fields or equivalent with significant post-doctoral experience
  • 15+ years of relevant employment or 20+ years with a Master's degree
  • 5+ years of supervisory or management experience
  • Strong knowledge of clinical pharmacology and pharmacometrics
  • Expertise in drug development and regulatory interactions

Responsibilities

  • Define scientific direction for Clinical Pharmacology plans
  • Provide strategic leadership to Clinical Pharmacology functions
  • Manage teams of Clinical Pharmacologists to set strategy and execute plans
  • Direct efforts for biologics and novel modality programs
  • Oversee human resource responsibilities for assigned staff

Benefits

  • Hybrid work flexibility allowing remote work
  • Integration with Global Research and Development for broader impact
  • Opportunity to lead cross-functional teams in clinical development
  • Direct involvement in shaping innovative drug strategies
  • Engagement in life-cycle management of drug development programs
Full Job Description

Job Description

General Summary:

The Senior Director, Clinical Pharmacology will serve as a Disease Area leader for Clinical Pharmacology. The Senior Director, Clinical Pharmacology will also manage the scientific functions and coordinate the activities of the Clinical Pharmacology function in collaboration with the other Disease Area leaders. The role’s responsibilities will include maintaining organizational processes across the group, influencing clinical program strategy, and integrating activities with other departments across the Global Research and Development organization, to help shape innovative and integrated clinical development plans. As a Disease Area leader, the Senior Director, Clinical Pharmacology will also direct Clinical Pharmacology efforts for biologics and other novel modality programs in the Disease Area.

Key Duties and Responsibilities:

  • Defines the scientific direction and directs the execution of clinical pharmacology plans for Disease Area programs
  • Provides strategic operational leadership to the Clinical Pharmacology function in collaboration with the other Disease Area Leaders
  • Manages a group of Clinical Pharmacologists at Director-level and below to set strategy, develop and execute Clinical Pharmacology plans and studies for Disease Area programs
  • Directs Clinical Pharmacology efforts for biologics/large molecule and novel modality programs in the Disease Area.
  • As a people manager within the organization, may have financial accountabilities and human resource responsibilities for assigned staff.

Knowledge and Skills:

  • Experience designing clinical pharmacology and pharmacometrics components of filing packages and associated clinical studies
  • Experience with regulatory agency interactions including written responses and IND packages
  • Experience with End of Phase 2 and NDA/MAA regulatory
  • Support of drug development programs in all Phases including life-cycle management
  • Experience with biologics/large molecule programs/assets
  • Experience leading cross-functional teams
  • Superior communication skills
  • Ability to solve complex problems while working in a matrix environment
  • Academic or clinical postdoctoral training with significant publication history

Education and Experience:

  • Ph.D. or Pharm D (or equivalent degree) in pharmacokinetics, pharmacometrics, clinical pharmacology or translational development and 15+ years of relevant post-doctoral employment experience, or
  • Masters Degree (or equivalent degree) in pharmacokinetics, pharmacometrics, clinical pharmacology or translational development and 20+ years of relevant employment experience, or
  • Typically requires 5 years of supervisory/management experience

#LI-KM4

Pay Range:

$232,000 - $348,000

Flex Designation:

Hybrid-Eligible Or On-Site Eligible

Flex Eligibility Status:

In this Hybrid-Eligible role, you can choose to be designated as: 
1.    Hybrid: work remotely up to two days per week; or select
2.    On-Site: work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time. 

#LI-Hybrid

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