Summit Therapeutics

Executive Medical Director

Princeton, NJ · Director

Sponsorship not specified$291k-$364kDetected 37 days ago

Clinical TrialsFDA Regulatory

About the role

We are seeking a physician to serve as a Medical Director to oversee global Phase 3 clinical trials and BLA (Biologic Licensing Application) filings.
Medical insight across a myriad of functions from discovery to manufacturing are expected.
The Medical Director will serve as a leader on one multiple potentially pivotal programs.

Manage direct reports or cross functional team members as needed based on team needs
Directing human clinical trials, Phases 1-3, for lead candidate in development, helping to ensure all clinical development milestones are met including enrollment goals.
Coordinate and develop information for reports submitted to FDA, EMA, PMDA, and government, regulatory, or partner agencies?
Knowledge of clinical trial conduct to support operational needs for planning and executing clinical trials, including adherence to protocols, safety reviews, assay development, training, and clinical document review

Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy.
Summit is headquartered in Miami, Florida, and has additional offices in California, New Jersey, the UK, and Ireland.
Prior experience in a mid-sized, fast-growing pharmaceutical environment is preferred, as this role will be working on product development in an extremely fast paced and intense environment.

Board certified or eligible MD with hematology/oncology product development and experience across stages of clinical development
Working knowledge of clinical development pathways for hematology/oncology therapeutics in the US and EMA
This is the pay for this position
Pay Transparency
$291,000 - $364,000 USD
This may be different in other locations due to differences in the cost of labor.
The total compensation package for this position may also include bonus, stock, benefits and/or other applicable variable compensation.
Summit does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site.
Summit Therapeutics Inc. is an Equal Opportunity Employer and takes pride in creating and maintaining diverse environment.

$291,000 - $364,000 USD
Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location.
This may be different in other locations due to differences in the cost of labor.
The total compensation package for this position may also include bonus, stock, benefits and/or other applicable variable compensation.
Summit does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site.
All employment businesses/agencies are required to contact Summit's Talent Acquisition team at recruiting@smmttx.com to obtain prior written authorization before referring any candidates to Summit.

Work cross functionally with Medical Affairs, Regulatory, Commercial and other functions to develop the overall product strategy in multiple indications.
Lead teams to execute on clinical development goals (clinical trial execution, clinical development strategy, medical affairs planning)
Participating in medical review of adverse event reports and monitoring of incoming safety data in conjunction with product safety/pharmacovigilance, including evaluating and escalating safety signals

This listing is sourced directly from Summit Therapeutics's careers page and normalized into a canonical job model.