Regulatory Project Manager
Remote
Competitive Pay & Benefits
Job Summary:
We are seeking a detail-oriented Regulatory Project Manager to oversee and monitor the evolving clinical trial regulatory landscape, ensuring compliance and strategic preparedness. This role requires strong research, analytical, and strategic thinking skills to assess regulatory changes, conduct impact analyses, and develop response strategies. The ideal candidate will have experience in market research, drug development, and regulatory policy within the life sciences or pharmaceutical industry.
Key Responsibilities:
- Monitor and analyze changes in clinical trial regulations, identifying potential impacts on business operations.
- Conduct market research and track industry trends, policy updates, and regulatory requirements.
- Develop and implement response strategies to regulatory changes, ensuring compliance and risk mitigation.
- Research and synthesize information from public websites, regulatory agencies, and industry sources.
- Collaborate with cross-functional teams to align regulatory insights with drug development processes.
- Provide guidance on process improvements and policy updates based on emerging regulations.
Qualifications:
- Bachelor’s or Master’s degree in Life Sciences, Regulatory Affairs, Public Policy, or a related field.
- Experience in regulatory research, clinical trials, or drug development.
- Strong strategic and critical thinking skills to assess regulatory impacts.
- Excellent research and analytical capabilities.
- Ability to interpret and communicate complex regulatory policies and market trends.
- Experience in process development and policy implementation is a plus.
