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.

For more information on this role please CLICK APPLY and forward your resume.