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Assistant Dmpk Jobs (NOW HIRING)

QPS, LLC

Receptionist / Administrative Assistant

Newark, DE ยท On-site

$19 - $20/hr

  • Life

  • Retirement

... DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II - IV ... The Job * Greet and assist visitors, employees, vendors, and callers in a professional and ...

New

Prime Medicine

Senior Scientist, Safety Assessment

Cambridge, MA ยท On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... DMPK, biodistribution, and delivery platform evaluation). * Contribute to evaluation of new delivery approaches, Lipid and RNA components, and emerging targets to support pipeline expansion. * Assist ...

QPS, LLC

Receptionist / Administrative Assistant

Newark, DE ยท On-site

$19 - $20/hr

  • Life

  • Retirement

... DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II - IV ... The Job * Greet and assist visitors, employees, vendors, and callers in a professional and ...

New

Inductive Bio

Product Scientist

New York, NY ยท On-site

$180K - $220K/yr

  • Medical

  • Dental

  • Vision

... assistant. Through a partnership with Enamine, we also offer library synthesis and direct-to-dose ... and DMPK expertise to real molecular optimization problems with a focus on dose-centric ...

QPS, LLC

Specialist, QuickBase Administration

Newark, DE ยท On-site

  • Life

  • Retirement

... DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II - IV ... Manage and implement database security and user accounts. * Assist with the design and development ...

QPS, LLC

PRN Logistics Technician

Springfield, MO ยท On-site

$18 - $22.50/hr

... DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Stage Clinical and Phase I IV Clinical ... Monitor inventory levels and assist with ordering laboratory and operational supplies * Assemble ...

New

Frontage Laboratories

Lab Technician

Exton, PA ยท On-site

$18.25 - $24.25/hr

  • Medical

  • Dental

  • Life

  • Retirement

... DMPK), pharmacodynamics (PD), bioanalytical services, safety and toxicology, Chemistry ... * Assist with sample receipt, logging, labeling, storage, retrieval, and chain-of-custody ...

Latigo Bio

VP, Toxicology

San Francisco, CA ยท Remote

Define target safety profiles and guide compound progression decisions in partnership with Discovery, DMPK, Clinical Pharmacology, and Clinical Development teams. Study Design & Execution * Design ...

Latigo Biotherapeutics

VP, Toxicology

San Francisco, CA ยท On-site

$310K - $340K/yr

Define target safety profiles and guide compound progression decisions in partnership with Discovery, DMPK, Clinical Pharmacology, and Clinical Development teams. Study Design & Execution * Design ...

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Senior Scientist, Safety Assessment

Prime Medicine

Cambridge, MA

Full-time

Re-posted 19 days ago

Job description

Position Overview

We are seeking an enthusiastic, self-motivated Senior Scientist to join the Nonclinical Development group, supporting the nonclinical safety assessment function for IND-enabling programs across Prime Medicine's pipeline. Reporting to the Associate Director, Safety Assessment, the successful candidate will support the design, execution, and interpretation of nonclinical safety studies conducted both in-house and at CROs, with an initial focus on liver-targeted therapeutics. This role requires hands-on involvement in assay execution and troubleshooting, as well as active participation in study oversight of work being done at CRO and data analysis.

This role requires collaboration within cross-functional teams. The ideal candidate will hold a Ph.D. in toxicology or a related field with 6+ years of pharma/biotech experience in nonclinical safety assessment, or an M.S. in toxicology or a related field with 10+ years of experience in nonclinical safety assessment, the ability to work independently, provide domain expertise and leadership, as well as cross-functionally in a fast-paced, matrixed environment with a positive, flexible attitude. ย ย 

Primary Responsibilities

  • Contribute to nonclinical safety activities as part of cross-functional Discovery and Development project teams, supporting program progression through IND-enabling stages.
  • Design, execute, and troubleshoot nonclinical safety studies, including hands-on laboratory work (~30%) to support assay development, data generation, and issue resolution.
  • Support the execution and oversight of nonclinical safety studies (GLP and non-GLP) at CROs, including active involvement in troubleshooting assay and study-related challenges.
  • Analyze and interpret study data with guidance and contribute to the preparation of study reports and supporting documents for regulatory submissions.
  • Collaborate with Pharmacology, DMPK, and other functions to support exploratory studies (e.g., exploratory toxicology, DMPK, biodistribution, and delivery platform evaluation).
  • Contribute to evaluation of new delivery approaches, Lipid and RNA components, and emerging targets to support pipeline expansion.
  • Assist in identifying potential safety findings and contribute to discussions on data interpretation and next steps.
  • Ensure studies and internal activities are conducted in compliance with regulatory guidelines and internal standards.

Preferred Qualifications

  • Ph.D. in toxicology or a related discipline with 6+ years of biopharmaceutical industry experience, or M.S. in toxicology or a related field with 10+ years of relevant biopharmaceutical industry experience supporting drug development in nonclinical safety/toxicology.
  • Experience in large molecule therapeutic development, along with a background in immunology, is desirable.
  • Understanding of toxicology principles, nonclinical safety evaluation, and the drug development process, with some experience interpreting toxicology data and contributing to technical and scientific reports.
  • Demonstrates strong scientific judgment and leadership with the ability to evaluate information, identify potential issues, and propose practical solutions with guidance as needed.
  • Highly organized and detail-oriented with strong attention to accuracy and quality.
  • Strong communication and collaboration skills, with the ability to work effectively across multidisciplinary teams and with external partners.
  • Experience supporting nonclinical studies at CROs is preferred but not required.

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