Clinical Regulatory Affairs Specialist
7 days ago
About GForce Life Sciences
GForce Life Sciences is a dynamic and innovative company that values the safety and effectiveness of its products. We are seeking a highly skilled Clinical Regulatory Affairs Specialist to join our team.
Estimated Salary: $110,000 - $140,000 per year
Job Description:
We are looking for a seasoned Clinical Regulatory Affairs Specialist to provide critical reviews of promotional pieces to ensure medical accuracy and validity. The successful candidate will have a strong understanding of the US pharmaceutical industry and healthcare landscape, as well as relevant guidance and compliance requirements.
Responsibilities:
- Determine the appropriateness of data and references used to support promotional claims and marketing messages, providing proactive recommendations and/or guidance for alternative data/references/language where needed.
- Align and collaborate with key cross-functional stakeholders on issues or concerns related to promotional materials or claims, engaging with commercial business partners early in the development of promotional materials to enhance efficiency.
- Provide critical analysis and application of scientific data in a customer-focused manner, ensuring safe and effective use of products by patients and the medical community.
Required Skills and Qualifications:
- PharmD / MD/ DO / NP with a minimum of two years of relevant professional experience; post-doctoral fellowship may be substituted for professional experience, as appropriate.
- Thorough understanding of the US pharmaceutical industry and healthcare landscape, promotional review process, and relevant guidance and compliance requirements.
- Ability to critically analyze and apply scientific data in a customer-focused manner.
Benefits:
- Competitive salary range.
- Opportunities for career growth and professional development.
- A dynamic and collaborative work environment.
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