Director, DMPK

Foghorn TherapeuticsWatertown, MA
13h$200,000 - $240,000

About The Position

This position offers an exciting opportunity to be a key part of a research and development organization that is pioneering a new class of medicines. The Director, DMPK project representative, will provide direct support to multiple project teams across the discovery and early clinical development portfolio.

Requirements

  • PhD or equivalent in relevant field
  • 7+ years of experience in pharmaceutical/biotechnology setting
  • Strong understanding of DMPK principles and ADME/PK assays in drug development
  • Demonstrated expertise in human PK and dose projections
  • Proven track record as DMPK project representative/leader on multiple project teams
  • Up-to-date knowledge of regulatory guidance related to ADME/PK characterization, drug-drug interaction, and human ADME studies
  • Experience with IND preparation and other regulatory documents
  • Strong communication and collaboration skills with ability to effectively convey ADME/PK risks
  • Demonstrated ability to work effectively in cross-functional team environments

Nice To Haves

  • Experience with covalent modalities, PROTACs and parenteral delivery preferred

Responsibilities

  • Design and execute issue-driven ADME/PK studies to address critical discovery project needs, supporting program progression through lead optimization to early development
  • Analyze and interpret preclinical ADME/PK data, communicating results and recommendations to project teams effectively
  • Build and maintain strong collaborations with internal and external partners across chemistry, biology, pharmacology, CMC and other R&D disciplines
  • Partner with discovery and clinical groups to design preclinical studies that inform clinical dosing strategy
  • Contribute to key decisions including candidate selection, development strategy, and clinical trial design
  • Author and review preclinical study reports, including nonclinical toxicology, DMPK and biomarker sections of regulatory documents
  • Design and interpret PK/PD, efficacy and toxicology studies in collaboration with cross-functional teams
  • Stay current with DMPK scientific literature and emerging technologies to identify potential applications for ongoing programs
  • Help finalize clinical study protocols and reports with focus on DMPK aspects

Benefits

  • Highly competitive and inclusive medical, dental and vision coverage options
  • BCBS PPO and PPO HSA plans
  • BCBS Dental Plan
  • EyeMed Vision Plan
  • FSA and HSA for medical expenses and dependent care expenses
  • 401(k) Program via Fidelity with the company match
  • Corporate Wellness Program
  • Unlimited Paid Time Off policy
  • Winter shut down
  • 12 weeks of 100% paid parental leave for birthing/primary parent and primary guardian in case of adoption and 3 weeks of 100% paid parental leave for non-birthing/non-primary parent/guardian.
  • Paid Life, LTD and STD insurance coverages, as well as voluntary benefit options
  • Free parking, subsidized commuter passes, or a $100 monthly stipend for walking/biking to work
  • Company lunches on Wednesdays

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What This Job Offers

Job Type

Full-time

Career Level

Director

Education Level

Ph.D. or professional degree

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