- Developing high-quality regulatory documents to support clinical trials and medical products
- Offering regulatory advice to optimize product development
- Aligning product development with global regulatory requirements and company strategy
- Serving as a liaison between the company and regulatory agencies
- Prior experience in Regulatory Affairs and Compliance, specifically in the pharmaceutical sector
- Proven track record in working with CTA and MA
- Providing scientific advisory assistance is a must
- Demonstrated ability in formulating regulatory strategy
- Familiarity with Regulatory Affairs laws and procedures
- Excellent communication and interpersonal abilities
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Regulatory Affairs Manager - Cambridge, United Kingdom - Park Street People
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Description
An innovative global pharmaceutical company is currently seeking a Regulatory Affairs Manager with CTA, UK/IE, and early stage development experience to join their team on a 12-month temporary contract.
As part of the regulatory team and working closely with key stakeholders, your main responsibility will be to provide regulatory strategy guidance and ensure timely approvals are met across the region.
Key responsibilities include:
Requirements:
Park Street People Ltd practices Equal Opportunities and adheres to UK legislation, ensuring no discrimination based on various factors.
We are operating as an Employment Business for this opportunity.