Chief Medical Officer
Barrington James · United States
Contract
Posted Nov 13, 2026
Job Description
My client is seeking an experienced, hands-on physician leader to support the clinical development strategy and execution of a biotech oncology program, with an initial focus on prostate cancer.
Key Responsibilities
Lead and contribute to clinical development strategy, initially focused on prostate cancer.
Review patient submissions and assess eligibility against protocol inclusion and exclusion criteria.
Provide hands-on medical monitoring and review patient safety information.
Develop, review, and refine clinical trial protocols.
Collaborate directly with investigators and site physicians on clinical questions, patient eligibility, and protocol interpretation.
Support clinical trial activities across a site network spanning across the US
Prepare and deliver presentations covering safety, clinical data, and program strategy.
Represent the company in scientific and clinical discussions with external stakeholders.
Combine senior-level strategic guidance with practical execution in a lean biotech environment.
Job Requirements
MD, Board Certified Oncology
Additional expertise in endocrinology or metabolic disease, particularly obesity or diabetes is highly desirable.
Experience in prostate cancer clinical development.
Direct biotechnology industry experience; large pharmaceutical company experience alone is not sufficient.
A hands-on working style, with the ability and willingness to execute clinical responsibilities rather than primarily delegate.
Experience reviewing clinical safety information, interpreting study data, and contributing to development strategy.
Ability to prepare and present slide decks on safety, clinical data, and strategic priorities.
Confidence and credibility representing the company to external stakeholders.
Strong communication skills and the ability to work closely with investigators, physicians, and company leadership.
Strong medical monitoring experience and willingness to undertake monitoring responsibilities alongside strategic work.
Start ASAP
10 hrs a week
12 months with a highly likely extension
Remote but open to travel to HQ and sites
Key Responsibilities
Lead and contribute to clinical development strategy, initially focused on prostate cancer.
Review patient submissions and assess eligibility against protocol inclusion and exclusion criteria.
Provide hands-on medical monitoring and review patient safety information.
Develop, review, and refine clinical trial protocols.
Collaborate directly with investigators and site physicians on clinical questions, patient eligibility, and protocol interpretation.
Support clinical trial activities across a site network spanning across the US
Prepare and deliver presentations covering safety, clinical data, and program strategy.
Represent the company in scientific and clinical discussions with external stakeholders.
Combine senior-level strategic guidance with practical execution in a lean biotech environment.
Job Requirements
MD, Board Certified Oncology
Additional expertise in endocrinology or metabolic disease, particularly obesity or diabetes is highly desirable.
Experience in prostate cancer clinical development.
Direct biotechnology industry experience; large pharmaceutical company experience alone is not sufficient.
A hands-on working style, with the ability and willingness to execute clinical responsibilities rather than primarily delegate.
Experience reviewing clinical safety information, interpreting study data, and contributing to development strategy.
Ability to prepare and present slide decks on safety, clinical data, and strategic priorities.
Confidence and credibility representing the company to external stakeholders.
Strong communication skills and the ability to work closely with investigators, physicians, and company leadership.
Strong medical monitoring experience and willingness to undertake monitoring responsibilities alongside strategic work.
Start ASAP
10 hrs a week
12 months with a highly likely extension
Remote but open to travel to HQ and sites
Additional Details
- City
- United States
- Country
- US
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