Medical Director

An innovative, growing biotechnology company is looking to bring on a Medical Director to support the clinical development of its hematology/oncology pipeline.

This is an excellent opportunity for a physician with a hematology/oncology background with at least one year of clinical development/clinical trial experience. The role will have a large impact on key programs for the organization, while remaining highly involved in the science, patients, and clinical development strategy.

What you’ll be doing:

• Serve as Medical Monitor for one or more interventional clinical trials
• Provide medical oversight of study conduct, patient safety, and emerging clinical data
• Review SAEs, AESIs, and other safety information alongside Pharmacovigilance
• Provide medical guidance to investigators, CROs, and study teams
• Support protocol development, eligibility reviews, protocol deviations, and subject management
• Participate in investigator meetings, site training, and data review meetings
• Collaborate closely with Clinical Operations, Clinical Development, Safety, Biometrics, Regulatory Affairs, and Medical Writing
• Contribute to regulatory submissions, clinical study reports, publications, and overall clinical development strategy
• Build relationships with investigators and key opinion leaders

What we’re looking for:

• 1-5 years industry experience, specifically in hematology or hematology/oncology
• 1+ years experience treating patients in clinical setting
• Experience with interventional clinical trials and clinical researchStrong understanding of GCP and clinical trial conduct
• Experience reviewing clinical/safety data and making medical decisions
• Phase I / early-phase clinical trial experience preferred
• Excellent communication and cross-functional collaboration skills

This is a hands-on opportunity for someone who wants to have a meaningful impact on clinical development rather than simply operate within a large, highly segmented organization.