Confidential
Executive Director and Vice President, Early Phase Clinical Development
Confidential, Detroit, Michigan, United States, 48201
Executive Director and Vice President, Early Phase Clinical Development
About the Company
Expanding biotechnology company
Industry Biotechnology
Type Privately Held
About the Role
The Company is in search of an Executive Director and Vice President for Early Phase Clinical Development. The successful candidate will be a Board-Certified Neurologist with a strong background in overseeing early clinical development projects, particularly in the area of autoimmune indications such as Multiple Sclerosis. This individual will be responsible for a portfolio of early-phase clinical development projects, designing and implementing clinical trial strategies, and leading cross-functional teams to ensure compliance with regulatory standards. The role also involves hands-on medical monitoring duties, SAE assessment, and managing external partners to ensure GCP compliance and the execution of deliverables.
Applicants must have a minimum of 3 years' of experience in biopharma/biotech, with a proven track record as a Lead Physician on an Asset Program. The position is an individual contributor role, reporting to the CMO, and is integral to the wider clinical team. The ideal candidate will have a strong scientific background, be adept at project management, and have a deep understanding of the regulatory landscape for early-phase clinical trials. The role is full-time and offers remote working within the USA.
Hiring Manager Title CMO
Travel Percent Less than 10%
Functions
Medical Care/Hospital Administration
About the Company
Expanding biotechnology company
Industry Biotechnology
Type Privately Held
About the Role
The Company is in search of an Executive Director and Vice President for Early Phase Clinical Development. The successful candidate will be a Board-Certified Neurologist with a strong background in overseeing early clinical development projects, particularly in the area of autoimmune indications such as Multiple Sclerosis. This individual will be responsible for a portfolio of early-phase clinical development projects, designing and implementing clinical trial strategies, and leading cross-functional teams to ensure compliance with regulatory standards. The role also involves hands-on medical monitoring duties, SAE assessment, and managing external partners to ensure GCP compliance and the execution of deliverables.
Applicants must have a minimum of 3 years' of experience in biopharma/biotech, with a proven track record as a Lead Physician on an Asset Program. The position is an individual contributor role, reporting to the CMO, and is integral to the wider clinical team. The ideal candidate will have a strong scientific background, be adept at project management, and have a deep understanding of the regulatory landscape for early-phase clinical trials. The role is full-time and offers remote working within the USA.
Hiring Manager Title CMO
Travel Percent Less than 10%
Functions
Medical Care/Hospital Administration