VP/Head of Clinical Pharmacology

EPM Scientific; Boston (MA); Remote; USD 180,000 - 250,000; Full time

Job summary

A pioneering oncology biotech company is seeking a Vice President of Clinical Pharmacology to lead their clinical pharmacology strategy. This role involves overseeing clinical studies, ensuring regulatory compliance, and developing a high-performing team to support their innovative therapies in cancer treatment. The candidate should have extensive experience in oncology and leadership within the pharmaceutical industry.

Benefits

Competitive salary and equity compensation

Comprehensive health, dental, and vision insurance

401(k) with company match

Generous paid time off and holidays

Professional development opportunities

Qualifications

• Minimum 13 years in pharmaceutical/biotech industry, with 5+ years in senior leadership.
• Expertise in oncology pharmacology and understanding of regulatory requirements.
• Proven track record in leading clinical pharmacology teams.

Responsibilities

• Lead the clinical pharmacology team and drive the clinical development strategy.
• Oversee design and implementation of clinical pharmacology studies.
• Foster external relationships with experts and regulatory agencies.

Skills

Leadership

Collaboration

Data Analysis

Regulatory Expertise

Communication

Education

PhD or PharmD in Pharmacology, Pharmaceutical Sciences

Job description

Vice President/Head of Clinical Pharmacology

Location: REMOTE (East Coast Based Biotech)

About Us:

Our team is partnered with a pioneering oncology biotech company dedicated to developing innovative therapies to improve the lives of cancer patients. They are committed to advancing their oncology pipeline through cutting-edge research and clinical development.

Position Overview:

The Vice President of Clinical Pharmacology will play a critical role in leading and shaping the company's clinical pharmacology strategy. This leadership position involves overseeing the design, development, and execution of clinical pharmacology studies to support the progression of our investigational therapies through clinical trials. The VP will work closely with cross-functional teams, including clinical development, regulatory affairs, and project management, to ensure the successful advancement of our oncology pipeline.

Key Responsibilities:

• Leadership & Strategy: Lead and manage the clinical pharmacology team to drive the clinical development strategy, integrating pharmacokinetics (PK), pharmacodynamics (PD), and drug-drug interaction assessments into all stages of clinical trials.
• Clinical Study Design: Develop and oversee the design and implementation of clinical pharmacology studies (e.g., dose escalation, PK/PD modeling) for oncology drug candidates, ensuring optimal dosing strategies and evidence generation.
• Regulatory Compliance: Provide pharmacology expertise and strategic guidance to ensure clinical studies meet regulatory requirements and align with global health authority expectations (FDA, EMA, etc.).
• Collaboration: Work cross-functionally with clinical development, medical affairs, regulatory affairs, and translational medicine teams to support the design, execution, and interpretation of clinical studies.
• Data Analysis & Interpretation: Oversee the analysis and interpretation of clinical pharmacology data to provide insights into dose optimization, safety profiles, and clinical pharmacology models.
• External Relationships: Foster relationships with external scientific and clinical experts, KOLs (Key Opinion Leaders), and regulatory agencies to ensure best practices and stay updated with industry trends.
• Team Development: Build, mentor, and grow a high-performing clinical pharmacology team while fostering a culture of collaboration, innovation, and excellence.
• Clinical Trial Management: Work closely with project management teams to ensure the timely execution of clinical trials, manage budgets, and ensure resources are appropriately allocated.
• Publications & Presentations: Contribute to scientific publications and presentations at industry conferences to enhance the company's scientific reputation and communicate clinical pharmacology findings.

Qualifications:

• PhD or PharmD in Pharmacology, Pharmaceutical Sciences, or a related field.
• Minimum of 13 years of experience in the pharmaceutical or biotechnology industry, with at least 5 years in a senior leadership role in clinical pharmacology.
• Expertise in oncology pharmacology and a strong understanding of clinical trial design and regulatory requirements.
• Experience leading IND/NDA/BLA regulatory submissions
• Proven track record of leading and managing clinical pharmacology teams.
• Excellent communication, collaboration, and leadership skills.
• Ability to work in a fast-paced, dynamic environment and manage multiple priorities.

Benefits:

• Competitive salary and equity compensation
• Comprehensive health, dental, and vision insurance
• 401(k) with company match
• Generous paid time off and holidays
• Professional development opportunities