A clinical stage precision oncology business in Boston, MA requires an Executive Medical Director lead a team of Medical Directors in the advancement of therapies for solid tumors based on their proprietary CRISPR-based platform.
Responsibilities:
- Establish clinical development plans and deliver on program milestones, in partnership with clinical leadership.
- Work effectively with in a matrix environment with other functions.
- As a senior member of the clinical study physicians team, provide leadership, mentorship, and guidance to other team members.
- Serve as the Medical Monitor on one or more studies.
- Author and review clinical documents required for the conduct of clinical studies, such as clinical protocols, amendments, informed consent documents, investigator brochures.
- Author and review clinical sections of regulatory documents, including INDs, annual safety reports and briefing packages.
- Lead clinical engagement with IRBs and Ethics committees.
- Work closely with internal teams and CROs in execution of trials, and provide ongoing guidance to CRO for protocol-specific clinical issues, site problems, and recruitment strategies.
- Manage a team of Medical Directors.
Requirements
- M.D required, with board certification in oncology preferred.
- Minimum of 4 years in oncology drug development, including early phase experience, with majority in pharmaceutical environment; experience in solid tumor oncology drug development is required.
- Experience leading a team through execution of clinical development plans.
- Strong people leadership abilities.
The company is looking to hire an oncologist with a clear track record in leadership within a pharma environment. The are looking for a hybrid worker in their Boston office but will allow a lot of flexibility to that.
The company has significant sums on hand and important partnerships which will bring additional investment to develop their best in class therapies.
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