Senior Medical Director

Cogent Biosciences

1d•$320,000 - $375,000•Hybrid

About The Position

This is a unique opportunity for a highly motivated and talented physician to play a key role in the development of bezuclastinib, the lead Cogent molecule, in the GIST indication. You will be a key team member in the research and development organization and will be a vital part of helping to achieve the Cogent vision: to discover, develop, and commercialize best-in-class therapies that have a dramatic impact for patients with genetically defined diseases. Cogent is a place where your input matters -- you will have a direct impact on our science and will help to build our capability as a team. You will also shape the Cogent culture and be a part of a passionate, transparent, and collaborative work environment. Working on a cross-functional multidisciplinary product team, and leading clinical development subteams, you will drive the development strategy, the design of clinical trials, and take accountability for the execution of the clinical development plan in support of the overall asset strategy in the GIST indication. You would be involved in supporting life cycle management opportunities and further regulatory activities for bezuclastinib in GIST. Primary medical monitor responsibilities, including oversight of trial subject safety and clinical data review and interpretation is expected, potentially in collaboration with and supported by a clinical scientist.

Requirements

MD with experience in medical oncology highly preferred
Minimum of 4 years of experience in clinical development at a biotechnology or pharmaceutical company. Experience in late phase is highly preferred
Critical strategic thinking to guide the clinical development program and life cycle management activities
Significant knowledge and experience in the design and execution of clinical trials with experience in overseeing global clinical trials from design through execution. Experience with regulatory submissions is highly preferred.
Demonstrated experience in clinical research, including designing, planning and monitoring clinical trials, particularly Phases 2-3
A creative problem solver with the proven ability to work independently and collaboratively in a fast-paced, result oriented environment.
Outstanding communication skills (written and verbal, both formal and informal).
Strong interpersonal, organization, and planning and communication skills. Effective skills directed toward driving collaboration, achieving results, influencing, and reaching consensus across internal and external stakeholders
A working knowledge of biostatistics, data management, clinical operations, translational sciences, clinical pharmacology and other technical disciplines and processes intimate with the drug development process

Responsibilities

In collaboration with the Head of Clinical Development, provide strategic and medical leadership for the bezuclastinib clinical development program in GIST
Provide clinical and medical support to life cycle management activities in GIST as needed
Collaborate with commercial and medical affairs colleagues to support launch activities for bezuclastinib in GIST
Provide primary medical monitor responsibilities, including oversight of trial subject safety and clinical data review and interpretation for the Peak clinical trial.
Design, prepare and initiate study protocols and other required documentation in compliance with project plans, federal regulations, good clinical practice (GCP) and good medical practice.
Work collaboratively with matrix team members in trial execution and oversight. Provide support to the clinical trial study team to manage safety, site education, protocol-related and eligibility questions.
Provide medical oversight and input into clinical trial documents including but not limited to the study protocol, informed consent form (ICF), statistical analysis plan (SAP), case report form (CRF), clinical study report (CSR)
Provide medical and scientific input into other documents including but not limited to the investigators’ brochure, regulatory filings and submissions, abstracts, manuscripts and publications, clinical study reports, etc.;
Collaborate with the regulatory team to develop briefing documents and other regulatory documents in support of submissions
Interact with clinical trial sites, external clinical experts, contract research organizations (CROs) and regulatory agencies, as needed.
Support investigator meetings, steering committee meetings, data monitoring committee reviews as the study physician.
Assist with regulatory submissions by answering protocol-related questions from regulatory authorities, ethics committees and institutional review boards (IRBs)
You will work collaboratively with all stakeholders from internal cross functional team members to external consultants, CRO partners, key opinion leaders, investigators, and various committee members.
You will develop a deep understanding of the clinical and competitive environment and work with the asset team to develop the target product profile