Regulatory Affairs Director

2 weeks ago


London, Greater London, United Kingdom Lifelancer Full time

MCRA, a leading medical device advisory firm and clinical research organization (CRO), offers an exciting opportunity for a Manager, Regulatory Affairs. Based in Europe, this critical team member will support regulatory strategy and submissions for clients across various therapeutic areas.

As a key player in our regulatory team, you will be responsible for developing and executing regulatory services, including writing, reviewing, and managing regulatory submissions. You will work closely with senior staff to communicate with regulatory bodies and clients, ensuring seamless project execution.

To succeed in this role, you should possess a bachelor's degree in a scientific, engineering, or regulatory discipline, with a minimum of five years of experience in Regulatory Affairs related to medical devices. Your expertise should include writing and/or reviewing of regulatory submissions, as well as a strong understanding of clinical research and data analysis.

In addition to your technical skills, you should be able to lead projects with minimal oversight, taking initiative and ownership of results while demonstrating self-accountability. Excellent organizational and prioritization skills are essential, along with the ability to handle multiple tasks and meet deadlines.

Lifelancer, a talent-hiring platform connecting professionals with opportunities in life sciences, pharma, and IT, invites applications for this position. If you're passionate about regulatory affairs and eager to contribute to a dynamic team, we encourage you to apply.



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