Regulatory Affairs Specialist
3 weeks ago
Job Summary
We are seeking a highly skilled Regulatory Affairs Specialist to join our team at 1925 GlaxoSmithKline LLC.
About the Role
As a Regulatory Affairs Specialist, you will be responsible for ensuring the development of appropriate Precision Medicine and Digital Health regulatory strategy(s) and their execution for assigned precision medicine and digital health asset(s) supporting across the GSK therapeutic portfolio.
Key Responsibilities
- Develop and execute global Precision Medicine and Digital Health regulatory strategy(s) for assigned precision medicine and digital health asset(s) supporting across the GSK therapeutic portfolio.
- Ensure compliance with regulatory requirements at all stages of product life from C2MD.
- Communicate effectively with cross-functional teams, including Regulatory, Clinical, and Medical Affairs.
Requirements
- Master's Degree in biological science, healthcare science, or engineering.
- Experience in regulation of companion diagnostics and SaMD.
- Proven ability to work in a matrix environment and lead cross-functional teams.
Preferred Qualifications
- Excellent communication and interpersonal skills.
- Proven ability to work in a fast-paced environment and prioritize multiple tasks.
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