Job Description

• Lead global regulatory DMPK strategy at a top CRO with broad industry exposure.
• Flexible remote role with international impact.

About Our Client

Our client is a globally recognized partner to the pharmaceutical and biotechnology industries, providing scientific expertise and integrated drug development services across multiple therapeutic areas and stages of development.

With a strong international presence and a collaborative, science-driven culture, our client delivers broad impact and the opportunity to work on innovative programs.

Job Description

• Serve as the DMPK regulatory subject matter expert supporting global drug development and submission strategies.
• Provide guidance on DMPK content for IND, NDA, and other regulatory submissions across multiple regions.
• Advise project teams on study design, data interpretation, and regulatory expectations for drug development programs.
• Engage with health authorities on DMPK-related topics, including regulatory meetings and written responses.
• Advise cross-functional teams and contribute expertise to client discussions, proposals, and business growth initiatives.
• Mentor scientists and project teams on regulatory strategy, submission best practices, and emerging industry trends.
• Represent the organization through publications, conference presentations, and participation in industry groups.
• Monitor evolving regulatory requirements and help ensure development programs remain aligned with global standards.

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on one's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.

The Successful Applicant

A successful Senior/Executive Director, DMPK should have:

• PhD in a related field and 20+ years of Drug Metabolism and Pharmacokinetics experience within the biopharmaceutical industry.
• A strong track record supporting successful IND, NDA, or comparable regulatory submissions.
• Extensive experience interacting directly with global health authorities, including the FDA and EMA.
• Deep expertise in DMPK strategy, study design, data interpretation, and regulatory documentation.
• An ability to advise cross-functional teams and provide expertise to client-facing initiatives across global programs.

What’s on Offer

• Base salary between $230,000 and $275,000 with bonus structure.
• Comprehensive health and life insurance coverage, and a 401k plan.
• Remote work ability within the United States.

If you are a DMPK expert looking for a role that blends scientific expertise with external stakeholder engagement and business impact, apply today.

Contact

Todd Jamison

Quote job ref

JN-082026-7076128

Job Tags

Permanent employment, Local area, Remote work, Flexible hours

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