Hematology Medical Director, Clinical Trials Leader

Treeline; Watertown (MA); On-site; USD 302,000 - 371,000; Full time

Job summary

Treeline Biosciences in Watertown, MA, seeks a Medical Director to provide medical oversight for assigned clinical trials, acting as the primary medical resource for investigators and study teams. You will ensure participant safety, support protocol execution, and review data in line with GCP and regulatory requirements.

This role involves collaboration across Clinical Development, Clinical Operations, Safety and Regulatory Affairs, contributing to high-quality study conduct and scientific

Qualifications

• MD required; board certification or board eligibility in hematology/oncology.
• 5+ years of clinical experience and/or pharmaceutical/biotech industry experience.
• Experience as Medical Monitor or Medical Director for interventional trials.
• Experience supporting Phase 1 studies in hematology/oncology preferred.

Responsibilities

• Act as medical monitor for one or more studies.
• Review safety data and provide medical guidance to sites and CROs.
• Support protocol development, informed consent and study materials.
• Review clinical data for consistency and subject safety.
• Participate in data review meetings and database lock activities.
• Collaborate with Clinical Operations, Biometrics, Medical Writing, Regulatory Affairs and Pharmacovigilance.
• Contribute to regulatory submissions and health authority responses.
• Prepare clinical study reports and publications.

Skills

ICH-GCP

FDA regulations

Medical monitoring

Clinical data review

Cross-functional collaboration

Communication skills

Attention to detail

Independence

Education

MD

Hematology/Oncology board

Job description

Treeline Biosciences in Watertown, MA, seeks a Medical Director to provide medical oversight for assigned clinical trials, acting as the primary medical resource for investigators and study teams. You will ensure participant safety, support protocol execution, and review data in line with GCP and regulatory requirements.

This role involves collaboration across Clinical Development, Clinical Operations, Safety and Regulatory Affairs, contributing to high-quality study conduct and scientific