Senior Director, Clinical Research job in Wilmington, USA

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

Job type: Contract

Discipline: VP/Head of Clinical Operations

Location: United States

This vacancy has now expired. Please see similar roles below...

Senior Director of Clinical Research - Contract - Wilmington, DE

Proclinical is seeking a dedicated and innovative individual for the role of Senior Director, Clinical Research.

Primary Responsibilities:

This role involves collaborating with physicians within Clinical Development to provide clinical research support for various programs. The successful candidate will be instrumental in developing protocols for clinical studies, contributing to program strategy, and maintaining updated knowledge of the competitive landscape.

Skills & Requirements:

Degree in a scientific/life sciences field. Pharm.D. or Ph.D. preferred.
Experience in research, preferably in drug development.
Prior experience in IAI and/or Dermatology drug development is preferred.
Ability to work independently, multi-task, and thrive in a fast-paced environment.
Excellent written and oral communication skills and strong analytical ability.
Willingness to travel up to 20% or as business dictates.

The Senior Director of Clinical Research's responsibilities will be:

Develop protocols for clinical studies.
Contribute to the development of program strategy for assigned compounds/programs.
Create and review clinical scientific documents such as IND, IND amendments, Investigator Brochures, Annual Reports, and other Health Authority submissions.
Provide clinical input into the design of eCRFs, SAP, and TLFs.
Collaborate with study team members to conduct timely and thorough reviews of study data.
Represent clinical development on project teams.
Develop relationships with consultants and external experts to obtain feedback on protocol design.
Act as the clinical lead for study abstracts, posters, oral presentations, and manuscripts for assigned studies.
Serve as a liaison to project teams, CROs, clinical sub-teams, and others.
Maintain updated knowledge of the competitive landscape regarding assets with similar MOA and/or evolving standards of care for indications of interest.

If you are having difficulty in applying or if you have any questions, please contact Mike Raletz at m.raletz@proclinical.com

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.