Regulatory Affairs Specialist

3 weeks ago


Chester, Cheshire, United Kingdom Planet Pharma Full time
About the Role

We are seeking an experienced Project Coordinator to join our team at Planet Pharma. In this critical position, you will provide crucial support to the Project Manager in managing clinical trials, ensuring that all processes run smoothly and efficiently.

Your primary responsibilities will include coordinating the engagement with regulatory agencies, assisting in drafting presentations and creating visual aids, and supporting the team in ensuring regulatory requirements and company policies are followed.

To excel in this role, you must possess excellent organizational skills, attention to detail, and the ability to work collaboratively as part of a dynamic team. A bachelor's degree in a relevant field, such as life sciences or project management, is required, along with 2+ years of experience in a similar position.

This role offers a generous salary of around $85,000 annually, comprehensive benefits, and opportunities for career growth and professional development.



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