Remote Director, Clinical Science — Phase 1–3 Leadership

BioAge Labs; United States; Remote; USD 230,000 - 250,000; Full time

Benefits offered by this job

Remote work

Health benefits

401(k) with match

Paid time off

Childcare benefits

Fertility benefits

Job summary

BioAge Labs is seeking an experienced Director of Clinical Science to lead Phase 1–3 trials, oversee protocol development, medical monitoring, patient safety reviews, and day-to-day trial execution in a fully remote role across the continental US.

Reporting to the Senior Director of Clinical Science, you will integrate preclinical, translational, biomarker, and clinical data to guide program decisions, collaborate with CROs and investigators, and contribute to regulatory submissions and study

Qualifications

• Doctor of Pharmacy (PharmD) or equivalent advanced degree required.
• Active pharmacist or medical licensure preferred but not required.
• 5+ years of progressive experience in clinical drug development.
• Experience supporting Phase 1–3 trials and medical monitoring.
• Experience authoring clinical protocols, SDSs, and regulatory documents.
• Experience interacting with investigators, CROs, and cross-functional teams.

Responsibilities

• Provide scientific and clinical leadership for Phase 1–3 trials including first-in-human studies.
• Oversee protocol development, medical monitoring, and patient safety reviews.
• Lead preparation of clinical study reports and regulatory submissions.
• Collaborate with Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, and Program Management.
• Coordinate with Pharmacovigilance on safety events and data review.

Skills

Clinical pharmacology

Medical monitoring

Protocol design

Regulatory submissions

Cross-functional leadership

Education

PharmD or equivalent advanced degree

Active pharmacist licensure preferred

Tools

NONMEM

Phoenix WinNonlin

Monolix

R

PBPK platforms

Job description

BioAge Labs is seeking an experienced Director of Clinical Science to lead Phase 1–3 trials, oversee protocol development, medical monitoring, patient safety reviews, and day-to-day trial execution in a fully remote role across the continental US.

Reporting to the Senior Director of Clinical Science, you will integrate preclinical, translational, biomarker, and clinical data to guide program decisions, collaborate with CROs and investigators, and contribute to regulatory submissions and study