Pre/Clinical Project Lead

By | September 11, 2025

Pre/Clinical Project Lead

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Job ID: 9907996

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Atlanta, GA, US

Scientific

Bachelors Degree

Full Time, Temporary

$50-$75/hour

Experienced (Non-Manager)

Remote

Biotechnology/Pharmaceuticals

First Shift (Day)

Atlanta, GA, US

$50-$75/hour

Experienced (Non-Manager)

Full Time, Temporary

Biotechnology/Pharmaceuticals

Remote

Scientific

Bachelors Degree

First Shift (Day)

Apply Now Applied

Job details

Job Title: Drug Development Project Manager / Scientific Program Manager

Industry: Biotechnology / Pharmaceutical R&D
Location: Remote or Hybrid (U.S.-based) Atlanta Metro area desired

Job Description

Dynamic and collaborative role supporting early-stage drug development programs from discovery through preclinical and into early clinical phases. This position serves as an extension of emerging biotech clients’ internal R&D teams, providing strategic guidance, scientific oversight, and hands-on program execution across a range of therapeutic areas.

Key Responsibilities

  • Program & Portfolio Management
    Oversee multiple drug development projects, coordinating timelines, deliverables, and stakeholder communications across cross-functional teams and external partners (CROs, CDMOs, regulatory consultants).


  • Preclinical Strategy & Execution
    Design and manage in vitro and in vivo studies, including toxicology, pharmacokinetics, and efficacy studies. Translate research findings into actionable plans aligned with development goals.


  • Regulatory Strategy Support
    Assist in preparation of regulatory submissions (e.g., pre-IND, IND), ensuring data packages are complete and compliant with FDA and global regulatory requirements.


  • Client & Partner Engagement
    Act as a scientific liaison between biotech clients and service providers, ensuring seamless execution and scientific rigor across all outsourced activities.


  • Data Analysis & Decision-Making
    Interpret and integrate data across multiple disciplines to support milestone decisions and go/no-go inflection points.

Key Areas of Focus

  • Small molecules, biologics, and novel therapeutics


  • Oncology, immunology, infectious disease, CNS, and metabolic disorders


  • IND-enabling studies and clinical trial readiness


  • U.S. and global drug development planning

Qualifications

  • Advanced degree (PhD, PharmD, or MS) in life sciences or related field


  • 5+ years of experience in biotech, pharma, or CRO environment, with hands-on program or project management


  • Strong understanding of preclinical development and regulatory pathways (especially IND processes)


  • Excellent communication and organizational skills


  • Ability to manage multiple projects and adapt in a fast-paced, client-facing environment

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