Senior Preclinical Program Manager

Neurocrine Biosciences

San Diego (CA)

On-site

USD 131,000 - 179,000

Full time

14 days+

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Benefits offered by this job

Health benefits
Retirement plan with company match
Equity incentive program

Job summary

Neurocrine Biosciences is seeking a Program Manager to lead Preclinical programs, spanning early research through IND/CTA readiness and First‑in‑Human development. You will partner with Toxicology, DMPK/ADME, Bioanalytical Sciences, Clinical Pharmacology, and Pharmacometrics, coordinating with Research, CMC, Clinical Development, Regulatory Affairs, and Finance to align strategy and execution.

The role requires strong program management, cross‑functional collaboration, and the ability to

Qualifications

  • Bachelor’s or higher with relevant experience in preclinical program management.
  • Experience spanning early research through IND/CTA readiness and FIH development.
  • Understanding of Toxicology, DMPK/ADME, Bioanalytical, Clinical Pharmacology, Pharmacometrics.
  • Ability to translate plans into integrated program timelines and milestones.
  • Strong cross-functional collaboration and communication with leadership.

Responsibilities

  • Provide program management leadership for 6+ Preclinical sub teams and coordinate across assets.
  • Develop and maintain integrated project plans, timelines, risk trackers, dashboards.
  • Monitor program performance and escalate issues to keep development objectives.
  • Support IND/CTA readiness and First‑in‑Human activities.
  • Participate in portfolio updates and leadership reporting.
  • Collaborate with Finance for budgeting and forecasting.
  • Identify opportunities for process improvements.

Skills

Program management
Cross-functional collaboration
Project planning
Risk management
Communication
Leadership

Education

Bachelor’s degree
Master’s degree
PharmD
PhD

Job description

Neurocrine Biosciences is seeking a Program Manager to lead Preclinical programs, spanning early research through IND/CTA readiness and First‑in‑Human development. You will partner with Toxicology, DMPK/ADME, Bioanalytical Sciences, Clinical Pharmacology, and Pharmacometrics, coordinating with Research, CMC, Clinical Development, Regulatory Affairs, and Finance to align strategy and execution.

The role requires strong program management, cross‑functional collaboration, and the ability to

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