Director, DMPK

Assembly Biosciences, Inc.

$228K — $252K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • PhD in chemistry, biochemistry, or related discipline with 10+ years of industry experience or equivalent Bachelors/Masters with added industry exposure.
  • Strong knowledge in ADME and PK/PD applied in small molecule optimization.
  • Exceptional understanding of drug metabolism, metabolic routes, and metabolite identification.
  • Expertise in both in vitro and in vivo DMPK methodologies for lead optimization in drug discovery.
  • Ability to collaborate across multiple disciplines and provide insightful guidance to chemists.
  • Demonstrated innovative research capabilities in DMPK relevant to drug candidate discovery.
  • Experience with regulatory documentation preparation, particularly for INDs and NDAs.

Responsibilities

  • Supervise external DMPK scientists to support R&D programs.
  • Provide scientific guidance on chemical lead optimization in collaboration with medicinal chemists.
  • Engage effectively with R&D teams for seamless communication.
  • Ensure thorough preclinical DMPK assessment for clinical candidates.
  • Analyze routes of elimination and the identity of metabolites as needed.
  • Support CTA and IND filing processes for clinical development.
  • Conduct PKPD modeling to inform discovery and development projects.

Benefits

  • Opportunities for professional development and advancement.
  • Collaborative environment focused on innovative research.
  • Engagement in meaningful work that impacts drug discovery.
  • Dynamic company culture within a fast-paced industry.
Full Job Description
POSITION SUMMARY

Position Title: Director, DMPK

Reports to: Executive Director, DMPK

Status: Regular, Full-time, Exempt

Location: South San Francisco, CA

Summary: We are seeking an experienced, creative, and highly motivated expert with industry research experience in DMPK focused on small molecule lead optimization for discovery research programs, preclinical and clinical drug development. In addition to overseeing a group of external professionals, this position will be responsible for leading DMPK interactions with medicinal chemists to facilitate the identification of molecules meeting criteria for clinical development and support preclinical and clinical development.

Specific responsibilities include, but are not limited to:
  • Supervising a group of external DMPK scientists supporting research and development programs.
  • Providing scientific guidance on chemical lead optimization programs and work in close collaboration with medicinal chemists to optimize the DMPK properties of candidate drugs.
  • Closely interacting and effectively communicating with individual research and development groups.
  • Ensuring complete preclinical DMPK assessment for clinical-stage candidate molecules.
  • Understanding routes of elimination, levels and identity of circulating metabolites and toxicology coverage as needed.
  • Supporting CTA and IND filings and contribute to clinical development for clinical candidates.
  • Performing PKPD modeling for discovery and development projects.
  • Scientific/technical aspects as well as management of assigned studies including protocol development, budget, timelines, oversight of outsourced activities, data analysis/interpretation and report writing.


This job description outlines the primary duties and responsibilities of the role; however, it is not intended to be all-inclusive. The scope of responsibilities may be modified, expanded, or adjusted at the discretion of the organization to meet evolving business needs.

Qualifications Include:
  • PhD in chemistry, biochemistry, or related discipline, with 10+ years of pharmaceutical industry experience. In lieu of a PhD, candidates who possess a Bachelor's or Master's degree with additional industry experience will be considered
  • A strong background in ADME and pharmacokinetics/pharmacodynamics as applied in small molecule lead optimization.
  • Exceptional knowledge of metabolic routes of biotransformation, metabolite identification and the chemistry of drug metabolism are required.
  • The candidate should have demonstrated technical knowledge and industrial experience in multiple DMPK areas and an in depth understanding of the experimental DMPK methodologies and approaches, in vitro and in vivo, utilized in chemical lead optimization.
  • The candidate must be able to work with multiple disciplines in drug discovery and provide exceptional guidance to medicinal chemists in the lead optimization process.
  • The candidate needs the ability to conduct innovative research in DMPK applied to the discovery of novel drug candidates to achieve defined milestones in a fast-paced environment.
  • The candidate should have extensive knowledge of preclinical drug development and may have experience in the preparation of regulatory documents, e.g. INDs and NDAs. In addition, she/he should be a goal oriented. Additional requirements include highly effective organizational and communication skills.
  • The candidate should be self-motivated, with a track record of productivity, demonstrated leadership potential, possess effective interpersonal skills and be team oriented.
  • The preferred candidate would also have experience and knowledge in Clinical Pharmacology.


Pay Range: $228,000 - $252,100 annualized

The stated pay range for this position reflects the San Francisco Bay Area job market. Assembly Bio establishes pay ranges based on geographic work locations. Additional factors such as academic credentials and relevant experience will influence the actual salary offered.

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