Executive Medical Oncology Director

Found in: Jooble US O C2 - 2 weeks ago


Boston MA, United States Verve Therapeutics Inc Full time

The Position
Verve is seeking a Medical Director, Clinical Development to join our team to advance highly innovative gene editing medicines for cardiovascular disease through clinical development. The successful candidate will collaborate with clinical operations to design and execute clinical studies of our gene editing medicines. The individual will represent the study through interactions with our internal teams, study investigators, key opinion leaders, and regulators. The individual will report to the Vice President of Translational Medicine and will have a highly visible position at the company. The ideal candidate will have outstanding communication skills, attention to detail, and the ability to thrive in a highly innovative and fast paced environment.
Job Responsibilities
Provide medical oversight of clinical trial activities including study design, study execution, and interpretation of emerging trial data
Contribute to the development of key study documents including the protocol and investigator’s brochure
Participate in the preparation of regulatory submissions and support responses to health authorities and ethics committees
Engage with study investigators and medical experts as part of the development of study protocols and study conduct
Collaborate with the research team to develop and implement a translational biomarker strategy for the program
Represent clinical development on cross-functional study teams
Travel to clinical sites, conferences, and regulatory meetings as needed
Qualifications
MD or MD/PhD with a minimum of 1 year of experience directly overseeing the conduct of clinical trials, preferably in an industry setting
Board eligible or certified in a medical specialty preferred
Strong clinical and scientific background with experience reviewing and interpreting study data.
Medical monitoring experience in clinical trials
Working knowledge of biostatistics, GCP, and regulatory requirements for clinical studies
Strong attention to detail and organizational skills
Exceptional verbal and written communication skills
Ability to work effectively with cross-functional teams
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