Director, DMPK

Our Culture: Why work with us?

At Foghorn Therapeutics, we believe in “People First, Mission Always.”

We put “People First” because we know our people are the key to everything we will accomplish. We value the diversity of background, ideas, perspectives and experiences that our team members bring to Foghorn Therapeutics – demonstrated by our community speaking more than 22 languages and representing over 24 nationalities. We value our teammates as people, not just as employees – validated by our actions that let our people know that we care about them, their families, and their lives.

We say “Mission Always” because we know a relentless commitment to our mission will make a difference in the lives of others. We believe our success will come from evaluating the data to follow the science. We work hard to develop a new class of therapies that could improve the lives of over 2.5 million people with cancer.

Our culture is focused on succeeding through the evaluation of data, not people. And in that, relationships can flourish and develop.

Our Science

The groundbreaking science behind our therapies continues to yield vital insights into diseases that have confounded physicians and researchers. Our core scientific approach is centered on the chromatin regulatory system, which opens and closes the right sections of DNA at the right time. Breakdowns in the chromatin regulatory system lead to a wide range of diseases, including cancer, impacting millions of people.

Our proprietary Gene Traffic Control® platform is a powerful tool for understanding and modulating the chromatin regulatory system. We are pursuing multiple treatments for breakdowns in this system. We are the only company with the ability to study and target the chromatin regulatory system at scale, in context, and in an integrated way.

The Role

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.

What You Will Be Doing

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

Requirements

About You:

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

Experience With Covalent Modalities, PROTACs And Parenteral Delivery Preferred

Demonstrated ability to work effectively in cross-functional team environments

Benefits

Foghorn Therapeutics is pleased to provide you and your family with a comprehensive suite of benefits, including:

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

Foghorn Therapeutics is a smoke-free, alcohol-free and drug-free work environment.

Foghorn is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. Foghorn Therapeutics will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

#LI-DNI

GatedTalent consolidates jobs from a variety of sources. Users of the “Talentis” and “FileFinder” executive search CRMs are able to publish jobs to the site with links from inside their core business apps. These are supplemented by jobs added by our own researchers and those provided by a third party job aggregation service. Please note that GatedTalent staff are not directly involved in the recruiting process.

Recruiting Brief

You don't have credit card details available. You will be redirected to update payment method page. Click OK to continue.