Hematology Medical Director: Clinical Trials & Safety Lead

Treeline Biosciences, Inc.; Massachusetts; On-site; USD 302,000 - 371,000; Full time

Job summary

Treeline Biosciences, Inc. is seeking a Medical Director to provide medical oversight for assigned clinical trials and act as the primary medical resource for investigators and study teams.

You will ensure participant safety, support protocol execution, review clinical data, and contribute to high-quality study conduct in line with GCP and regulatory requirements. You will collaborate across Clinical Development, Clinical Operations, Safety, Biometrics, Regulatory Affairs, and external partners

Qualifications

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

Responsibilities

• Provide medical oversight for assigned clinical trials and act as the primary medical resource for investigators and study teams.
• Review safety data and emerging clinical information; guide medical decisions on dose modifications and subject management.
• Collaborate across Clinical Development, Clinical Operations, Safety, Biometrics, Regulatory Affairs, and external partners to ensure efficient, compliant study conduct.
• Participate in protocol development, data reviews, study initiation, investigator meetings, and preparation of clinical study reports.

Skills

ICH-GCP

FDA regulations

Clinical data interpretation

Communication skills

Cross-functional collaboration

Biotech environment experience

Education

MD

Board certification or board eligibility in hematology/oncology

Job description

Treeline Biosciences, Inc. is seeking a Medical Director to provide medical oversight for assigned clinical trials and act as the primary medical resource for investigators and study teams.

You will ensure participant safety, support protocol execution, review clinical data, and contribute to high-quality study conduct in line with GCP and regulatory requirements. You will collaborate across Clinical Development, Clinical Operations, Safety, Biometrics, Regulatory Affairs, and external partners