Global Clinical Program Manager for Biotech Regulatory Affairs

4 days ago


Cambridge, Cambridgeshire, United Kingdom Lifelancer Full time
About Lifelancer

Lifelancer is a talent-hiring platform in Life Sciences, Pharma, and IT. We connect talented professionals with opportunities in pharma, biotech, health sciences, healthtech, and IT domains.

Job Title: Global Clinical Program Manager for Biotech Regulatory Affairs

We are seeking a highly skilled Global Clinical Program Manager for our Regulatory Affairs team. As a key member of our team, you will be responsible for managing clinical programs and ensuring compliance with regulatory requirements.

Responsibilities:
  • Develop and implement global clinical trial strategies to meet business objectives
  • Collaborate with cross-functional teams to ensure seamless execution of clinical trials
  • Maintain awareness of regulatory developments and updates in the life sciences industry
Requirements:
  • Degree in Law or related field
  • Proven experience in regulatory affairs, preferably in a biotech/pharmaceutical company
  • Excellent communication and project management skills
What You Can Expect:
  • A competitive salary of £80,000 - £110,000 per annum
  • A dynamic and supportive work environment
  • Ongoing training and development opportunities
Location:

This role can be based in our Cambridge office, with occasional travel required to other locations within the UK and abroad.

Apply now to take your career to the next level



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