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Associate Director Preclinical Research Jobs (NOW HIRING)

The Preclinical Evidence & External Partnerships Associate Director will drive pre-market evidence ... Manages the preclinical external research program and physician partnerships in coordination with ...

With the goal of further increasing the pace of progress towards better treatments, we're hiring a Director of Preclinical Research to help us pursue a growing number of research opportunities ...

Plan, direct, coordinate, and execute activities related to the design, initiation. and follow-up ... junior associates. * Administrater and manage Cresilon's preclinical regulatory strategy and ...

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How much do associate director preclinical research jobs pay per year?

As of Sep 10, 2026, the average yearly pay for associate director preclinical research in the United States is $102,728.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,000.00 and $141,000.00 per year, depending on experience, location, and employer.

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Infographic showing various Associate Director Preclinical Research job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $102,728 per year, or $49.4 per hour.

Preclinical Research Associate Director

Irvine, CA โ€ข On-site

Scorpion Therapeutics
51 - 200 employees

Other

Posted 2 days ago

New


Job description

Purpose:
  • The Preclinical Evidence & External Partnerships Associate Director will drive pre-market evidence generation strategies (EGS) and physician collaborations, generating clinically relevant evidence for the companyโ€™s pipeline.
You Will Be Responsible For:
  • Ideate preclinical evidence strategies to support first-in-human use for all portfolio programs.
  • Manage the preclinical external research program and physician partnerships with cross-functional clinical science partners.
  • Review new study proposals; ensure timely decisions and execution of approved studies with external stakeholders.
  • Use program data and metrics to conduct regular program reviews and provide updates to team leadership.
  • Support evidence generation and dissemination strategy, including publication plan alignment and identifying gaps.
  • Drive publication development with investigators and cross-functionally with Scientific Affairs partners; provide critical scientific input to publications.
  • Contribute to preclinical protocol development for all portfolio products.
  • Provide input to external physician partners on proposed preclinical research plans.
Qualifications / Requirements:
  • Bachelorโ€™s degree in Biological Science or related discipline (Masterโ€™s or PhD strongly preferred).
  • 8+ years related scientific/technical experience with leadership/management in Medical Affairs or similar role.
  • 2+ years people management experience.
  • Experience in Cardiovascular, Electrophysiology, or Structural Heart strongly preferred.
  • Expertise in preclinical science/processes; broad understanding of product development, clinical trends, and clinical trial regulations.
  • Experience supporting global regulatory submissions (IDE/510(k)/De Novo/PMA or global counterparts) highly desired.
  • Ability to lead preclinical scientists across NPD projects; proven track record delivering on time/budget and compliant with SOPs/regulations.
  • Up to 25% domestic/international travel.
Preferred Skills:
  • Analytical reasoning; clinical research & regulations; clinical trials operations; communication; developing others; digital literacy/culture; healthcare trends; inclusive leadership; leadership; medical affairs/communications/compliance; prioritization; product strategies; scientific research; strategic thinking; team management.
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