Director, Clinical Pharmacology

Posted 15 Days Ago
Be an Early Applicant
Boston, MA, USA
In-Office
200K-300K Annually
Expert/Leader
Biotech • Pharmaceutical
The Role
Leads clinical pharmacology strategy and operations across drug development programs. Develops clinical pharmacology plans, guides metabolic and drug-drug interaction studies, oversees protocol start-up, PK and PK/PD analyses, modeling and simulations, and regulatory and safety documentation. Represents the department on cross-functional teams, supervises staff, supports hiring and career development, and contributes to departmental and program-level decision-making.
Summary Generated by Built In

Job Description

General Summary:

The Director, Clinical Pharmacology leads strategic, scientific and operational aspects at a program level. This role represents the department on strategic and operational cross-functional program teams and will be responsible for the development of clinical pharmacology plans; assists in departmental management through program reviews and collaborative decision-making; supervises asset leads, provides career development; routinely co-leads cross-functional efforts and leads department initiatives.

Key Duties and Responsibilities:

  • Guides metabolic, co-dosing and drug-drug interaction issues, collaborating closely with cross functional colleagues
  • Co-leads or serves on cross-functional committees and/or contributes to or leads departmental initiatives
  • Creates protocol concepts and guides protocol start-up including site initiations and investigator meetings
  • Oversees and contributes to regulatory and safety documents
  • Contributes to clinical pharmacology summary documents
  • Guides PK analyses
  • Performs PK/PD or exploratory analyses and guides PK/PD modeling or simulations as appropriate
  • Provides management and career development to staff
  • Assists in recruitment and hiring
  • As a people manager within the organization, may have financial accountabilities and human resource responsibilities for assigned staff
  • Knowledge and Skills:

  • Knowledge expert in Clinical Pharmacology
  • Effective leadership skills to drive performance and provide career development opportunities to staff
  • Critical thinking skills, with keen scientific and development judgment
  • Experience planning and executing Clinical Development Plans for new clinical entities particularly as it applies to the discipline of Clinical Pharmacology
  • Experience conducting and supervising clinical studies such as drug-drug interaction, special population or bioavailability
  • Experience conducting and supervising non-compartmental pharmacokinetic (PK) and PK/pharmacodynamic analyses
  • Experience with a range of clinical studies including first-in-human, proof-of-concept and registrational studies
  • Experience contributing to clinical and regulatory documents such as the Investigator’s Brochure and contributing to regulatory correspondence
  • Experience working on teams and in a matrix environment
  • Education and Experience:

  • Ph.D. or Pharm D (or equivalent degree) in pharmacokinetics, pharmacometrics, clinical pharmacology or translational development and 10+ years of relevant post-doctoral employment experience, or
  • Masters Degree (or equivalent degree) in pharmacokinetics, pharmacometrics, clinical pharmacology or translational development and 15+ years of relevant employment experience
  • Typically requires 3 years of supervisory/management experience
  • Pay Range:

    $200,000 - $300,000

    Disclosure Statement:

    The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.

    At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.  From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.

    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
     

    Company Information

    Vertex is a global biotechnology company that invests in scientific innovation.

    Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

    Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at [email protected]

    Skills Required

    • Ph.D., Pharm.D., or equivalent degree in pharmacokinetics, pharmacometrics, clinical pharmacology, or translational development, plus 10 or more years of relevant post-doctoral employment experience
    • Alternatively, a master's degree or equivalent in pharmacokinetics, pharmacometrics, clinical pharmacology, or translational development, plus 15 or more years of relevant employment experience
    • At least 3 years of supervisory or management experience
    • Expert-level knowledge of clinical pharmacology
    • Experience planning and executing clinical development plans for new clinical entities
    • Experience conducting and supervising clinical studies, including drug-drug interaction, special population, or bioavailability studies
    • Experience conducting and supervising non-compartmental pharmacokinetic and PK/pharmacodynamic analyses
    • Experience with first-in-human, proof-of-concept, and registrational clinical studies
    • Experience contributing to clinical and regulatory documents, including Investigator's Brochures and regulatory correspondence
    • Experience guiding PK/PD modeling or simulations
    • Experience working in cross-functional teams and matrix environments
    • Effective leadership, critical thinking, and scientific and development judgment

    Vertex Pharmaceuticals Compensation & Benefits Highlights

    The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Vertex Pharmaceuticals and has not been reviewed or approved by Vertex Pharmaceuticals.

    • Parental & Family Support Policies provide 12 weeks of 100% paid bonding leave for all U.S. parents with additional fully paid time for birth parents. Family-forming supports include adoption and surrogacy assistance, fertility options like IVF and egg cryopreservation, breast‑milk shipping, subsidized childcare, backup care, and a DCFSA match.
    • Leave & Time Off Breadth Time off includes roughly four weeks of vacation, 13 holidays, sick time, and two companywide shutdowns (summer and year‑end). Some roles also include flexible or unlimited time off and paid volunteer time.
    • Retirement Support Programs include a 401(k) plan with employer contributions and an employee stock purchase plan. Filings describe employer contributions occurring in company stock, supporting long‑term ownership.

    Vertex Pharmaceuticals Insights

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    The Company
    HQ: Boston, MA
    5,000 Employees
    Year Founded: 1989

    What We Do

    Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious and life-threatening diseases. We discovered and developed the first medicines to treat the underlying cause of cystic fibrosis (CF), a rare, life-threatening genetic disease. In addition to clinical development programs in CF, Vertex has more than a dozen ongoing research programs focused on the underlying mechanisms of other serious diseases. Founded in 1989 in Cambridge, Massachusetts, our corporate headquarters is now located in Boston’s Innovation District, and our international headquarters is in London, United Kingdom. We currently employ approximately 3,500 people in the United States, Europe, Canada, Australia and Latin America with nearly two-thirds of our staff dedicated to research and development. Vertex is consistently recognized as one of the industry’s top places to work by Science Magazine, The Boston Globe, Boston Business Journal and the San Diego Business Journal. Our research and medicines have also received esteemed recognitions, including the Robert J. Beall Therapeutics Development Award, the French Prix Galien and the British Pharmacological Society awards.

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