Senior Clinical Research Physician — Early Development

100 Eli Lilly and Company

United States

Remote

USD 201,000 - 394,000

Full time

14 days+
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Job summary

Lilly seeks a Clinical Research Physician (CRP) to lead early clinical development with focus on clinical pharmacology across therapeutic areas. The CRP will advance assets into first‑in‑human studies and support biomarker strategies, regulatory submissions, and global trial execution.

The role requires strong medical training, regulatory knowledge, and cross‑functional collaboration. The candidate should have MD/DO credentials, board eligibility or certification, and 2+ years pharma experience

Qualifications

  • Medical degree and board eligibility or certification required.
  • Pharmaceutical industry experience preferred.
  • Experience in designing and conducting early phase clinical trials (Phase 1/2).
  • Fluent English, strong written and verbal communication.

Responsibilities

  • Contribute to development of overall clinical strategy and plan for early compounds.
  • Design and oversee clinical pharmacology studies (SA, bioavailability, DDI, biomarker plans).
  • Coordinate protocol development, risk assessment, and regulatory submission support.
  • Collaborate with cross-functional teams and external experts to advance program goals.
  • Ensure compliance with GCP, regulatory requirements, and company policies.
  • Monitor safety and oversee pharmacovigilance actions as needed.
  • Support publication and dissemination of clinical trial results.

Skills

Pharma industry
Clinical pharmacology
Phase 1 trials
Cardiometabolic
Communication skills

Education

MD or DO

Job description

Lilly seeks a Clinical Research Physician (CRP) to lead early clinical development with focus on clinical pharmacology across therapeutic areas. The CRP will advance assets into first‑in‑human studies and support biomarker strategies, regulatory submissions, and global trial execution.

The role requires strong medical training, regulatory knowledge, and cross‑functional collaboration. The candidate should have MD/DO credentials, board eligibility or certification, and 2+ years pharma experience

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