What are the responsibilities and job description for the Regulatory Affairs, Project Manager position at Proclinical?
Regulatory Affairs, Project Manager - Contract - Remote, Indianapolis
Proclinical is looking for a detail-oriented and strategic Regulatory Project Manager to support a project with one of our clients in their Clinical Trial Patient Engagement Team.
Primary Responsibilities :
This role is critical in monitoring the evolving clinical trial regulatory landscape and ensuring compliance with current regulations. The ideal candidate will conduct impact analyses, develop proactive response strategies, and stay updated on the latest drug development trends, policies, and regulatory changes to guide project decision-making. This is an opportunity to work with one of our clients in their Clinical Trial Patient Engagement Team, supporting innovative approaches to patient-centered clinical research.
Skills & Requirements :
- Minimum of 3 years of experience in regulatory project management, clinical trials, or drug development.
- In-depth knowledge of regulatory environments related to clinical trials and drug development.
- Proven experience in market research, policy analysis, and regulatory impact assessment.
- Exceptional attention to detail and the ability to manage multiple projects and priorities simultaneously.
- Excellent communication and interpersonal skills for interacting with cross-functional teams and stakeholders.
The Regulatory Affairs, Project Manager's responsibilities will be :
