Executive Director / VP, Clinical Pharmacology
US, Remote
Required Experience:
Clinical Pharmacology, 10+ years
Required Experience:
Clinical Pharmacology, 10+ years
- Team managment, +5 years
- Pharma Bio industry, 15+ years
Required Education:
PhD or Pharm D, preferred
Required Education:
PhD or Pharm D, preferred
Job Description
Executive Director / Vice President – Clinical Pharmacology
Confidential Clinical-Stage Biopharma (Oncology Focus)
Company Overview
- Therapeutic Area: Oncology, with emphasis on RAS- and Kinase-driven malignancies
- Stage: Clinical-stage, expanding rapidly across research, clinical, and translational functions
- Culture: Agile, science-driven, collaborative, with a mission-oriented focus on improving patient outcomes
Position Highlights
Title: Executive Director / Vice President, Clinical Pharmacology, Remote US
Location: Remote (U.S. based, with strong preference for major biotech hubs)
Compensation: $290,000 - $330,000 base + bonus, equity, and full benefits
Key Responsibilities
- Lead the clinical pharmacology strategy across multiple oncology programs, ensuring scientific rigor and regulatory alignment.
- Oversee the design and execution of clinical pharmacology studies, including first-in-human and proof-of-concept trials.
- Apply model-informed drug development (MIDD) approaches, including PBPK, PK/PD, population PK, and exposure-response analyses.
- Serve as regulatory lead for clinical pharmacology, authoring IND, CTA, NDA modules and engaging with FDA/global health authorities.
- Collaborate with cross-functional leaders in clinical operations, regulatory, biostatistics, and translational medicine to advance pipeline assets.
- Stay on the forefront of innovation in clinical pharmacology and oncology, contributing thought leadership to the field.
Ideal Candidate Profile
- Ph.D. or equivalent in Clinical Pharmacology, Pharmacokinetics/Pharmacodynamics, or related field
- 10-15+ years of experience in oncology clinical pharmacology, ideally with small molecules in solid tumors
- Strong track record of regulatory submissions and successful advancement of oncology programs into late-stage development
- Expertise in quantitative pharmacology (PBPK, exposure-response, population PK/PD)
- Excellent cross-functional leadership skills and ability to operate in a fast-paced biotech environment
Why This Role is Attractive
- Impact: Lead clinical pharmacology strategy in a company poised to change treatment paradigms in oncology
- Visibility: Direct interaction with executive leadership and global regulators
- Growth: Opportunity to shape multiple oncology programs and influence portfolio strategy
- Rewards: Competitive total compensation with equity participation in a high-growth biopharma
GRN Boston North
633 Waverly Road
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North Andover, MA 01845 USA