Executive / Senior Medical Director

Verastem•Boston, MA

31d

About The Position

We are looking for a n Executive / Senior Medical Director ( l eve l dependent on qualifications) to support our growing Clinical Development team! Reporting to the Vice President of Clinical Development. The position provides medical and scientific leadership for Verastem’s potentially best-in-class KRAS G12D ON/OFF inhibitor : VS-7375 P rogram. This individual will serve as the Clinical Lead for one or more studies to lead study execution and development strateg y , as well as being a key member of the Program Team to bring VS-7375 through development cycles and potential market authorization application s .

Requirements

Medical Degree (M.D. or equivalent) .
5 + years of experience in biotech / pharma industry o ncology drug development ( or substantial investigational therapeutics experience as a clinical investigator if not meeting industry experience requirement ) is
Knowledge of Good Clinical Practices ( cGCP )
comprehensive knowledge of clinical trial design
understanding of the overall global drug development process.
Knowledge of current external regulatory environment, e.g. FDA, EMA requirements
Ability to work independently and the exercise of good medical, clinical judgment in resolving critical problems not always covered by existing standards, policies and procedures.
Excellent interpersonal, verbal communication, and influencing skills.
A track record of leading cross-functional matrix teams.
Demonstrated ability to develop and cultivate relationships with key internal, and external, partners and stakeholders.
S trong analytical and presentation skills: effective at summarizing and presenting the key considerations and decision-points.
Comfortable working in fast paced entrepreneurial environment, with a flexible mindset to be successful in a biotech corporate culture .
Ability to travel up to 20% of the time.

Nice To Haves

Board-certified in oncology
Experience in GI oncology and/or lung cancer
With an established investigator / KOL network in oncology
NDA / BLA experience

Responsibilities

Support s the design and execution of assigned clinical trial (s) and works closely with cross functional study team members to execute activities associated with the conduct of the clinical trials.
Serves as the p rimary medical / safety contact for assigned clinical trials, ensuring compliance and patient safety.
Serve as the primary contact for medical-related inquiries from investigators, regulatory agencies, and internal/external teams, ensuring consistent protocol interpretation and clarification .
Partner s with Clinical Science , Data Management , Sta tistical Programing to ensure data integrity .
L ead regular data reviews and insight generation to guide development strategy .
Collaborate s with S afety on reporting of identified adverse events (AEs), serious adverse events (SAEs), and other safety-related events.
Contributes to safety profile characterization and corresponding risk mitigation strategy / plans .
A c t s as a key member of the Program Team to devise integrated development plan(s) and development / regulatory strategies.
Author s and develop key study and regulatory documents with the cross functional team, including, but not limited to study protocol, investigator brochure, informed consent form, and clinical study reports.
Contribute s to scientific publications, including conference abstracts and peer-reviewed journal articles.
Represent s the study / program and i nteract s on a regular basis with key internal / external partners and stakeholders, including key opinion leaders, clinical investigators, clinicians, scientists as well as internal leadership team and R&D .
L ead and present at investigator meetings and advisory committees.
Maintains scientific and clinical knowledge in oncology and provides input on Verastem’s pipeline, translational and preclinical work.