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Regulatory Affairs Specialist
1 month ago
We are seeking a highly skilled Regulatory Affairs Specialist to join our team in Cambridge or Uxbridge. The successful candidate will play a critical role in supporting the regulatory team and contributing to our mission to serve patients.
In this challenging position, you will be responsible for implementing the regional regulatory strategy and executing regulatory plans. You will prepare supporting documentation for regulatory submissions, including clinical trial applications, marketing authorizations, and lifecycle management activities.
Key Responsibilities:
- Implement regional regulatory strategies and execute regulatory plans.
- Prepare supporting documentation for regulatory submissions.
- Ensure compliance with regulatory requirements.
Requirements:
- Bachelor's degree (scientific area) and 2 years of directly related experience.
- Master's degree (scientific area).
Estimated Salary: £45,000 - £60,000 per annum.
About Us:
Planet Pharma is a leading provider of global staffing services, with a network of 2500+ active contractors globally. We specialize in areas like Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
