Director/Senior Director of DMPK
Posted on 3/22/2024
Genesis Therapeutics

51-200 employees

Combining AI and biotechnology for drug discovery
Company Overview
Genesis Therapeutics is on a mission to transform every stage of drug discovery to solve critical patient needs. The company is unlocking novel protein targets, exploring untapped chemical space, and accelerating the development of critical new medicines with the industry's most advanced molecular AI platform.
B2B

Company Stage

Series B

Total Funding

$256.1M

Founded

2019

Headquarters

Burlingame, California

Growth & Insights
Headcount

6 month growth

17%

1 year growth

17%

2 year growth

17%
Locations
San Diego, CA, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
CategoriesNew
Bioinformatics
Computational Biology
Biology Lab & Research
Biology & Biotech
Requirements
  • MSc or Ph.D. in Biological Science, Chemistry, Pharmacokinetics, Pharmacology or related discipline with 10+ years Industrial experience in Drug Discovery & Development
  • Verifiable track record of drug discovery experience, success, and leadership, with experience in advancing programs through all stages of discovery to IND candidates
  • Thorough knowledge of FDA and ICH guidelines
  • Knowledge of various in-vitro & in vivo ADME assays
  • Ability to work effectively in a dynamic environment with diverse team of coworkers
  • Solid written and oral communication skills, enthusiasm, integrity, self-motivation, strong interpersonal skills, and attention to detail are necessary
Responsibilities
  • Represent DMPK as an integral member of project/core teams, providing scientific and strategic leadership for all stages of drug discovery and early development
  • Lead the DMPK team (2-3 scientists) and built internal DMPK assay capabilities to support internal programs
  • Effectively manage CROs and DMPK team to design and execute in vitro and in vivo studies aimed at characterizing the DMPK/ADME properties of small molecule drug candidates
  • Communicate DMPK data and provide interpretation of results to project teams, senior management, and other stakeholders
  • Oversee the preparation of nonclinical DMPK/ADME reports and the relevant sections of documents for regulatory submissions
  • Provide input into the pharmacokinetic and design aspects of nonclinical pharmacology and nonclinical toxicology studies
  • Partner with AI engineer on ADME predictive model
  • Be a scientific leader and mentor