SonicJobs Logo
Login
Left arrow iconBack to search

Clinical Project Manager

SciPro
Posted a day ago, valid for 9 days
Location

Hitchin, Hertfordshire SG5 1EP, England

Salary

£50,000 - £60,000 per annum

info
Contract type

Full Time

By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.

Sonic Summary

info
  • The Clinical Operations Manager position is based in the UK with a hybrid work model of three days onsite and two days remote.
  • The role requires proven experience in managing or leading clinical trials, ideally in both pharmaceutical and medical device settings.
  • The successful candidate will oversee clinical operations across a diverse portfolio, including medicines, medical devices, and cosmetics.
  • This position emphasizes strategic oversight and hands-on delivery, particularly in post-market clinical investigations and MDR-related projects.
  • The salary for this role is competitive, reflecting the candidate's experience and expertise in the field.

Clinical Operations Manager

Location: UK (Hybrid – 3 days onsite, 2 remote)
 

SciPro are partnering with an exciting, privately owned pharmaceutical company who are seeking an experienced Clinical Project Manager to join their team in the UK. In the role, you will lead clinical operations across a diverse portfolio of medicines, medical devices, and cosmetics. The position offers an excellent balance of strategic oversight and hands-on delivery, with exposure to complex and varied clinical studies – particularly post-market clinical investigations and MDR-related projects.

The company pride themselves on their collaborative culture and commitment to scientific excellence, developing and marketing leading treatments. This is a unique opportunity to make a tangible impact in an agile, lean structure where your ideas and expertise will truly shape the future of their clinical programs. 

Key Responsibilities:

  • Oversee and manage the design, conduct, and delivery of clinical trials and post-market clinical investigations across medicines, medical devices, and cosmetics.
  • Lead and support a multidisciplinary clinical team, ensuring high-quality execution and compliance with regulatory requirements (including MDR).
  • Contribute to clinical strategy and continuous process improvement.

Key Requirements:

  • Proven experience managing or leading clinical trials, ideally within both pharmaceutical and medical device settings.
  • Strong people management and cross-functional collaboration skills, with the ability to influence and engage across departments.
  • Solid understanding of regulatory and clinical guidelines, risk assessment, and problem-solving in complex study environments.

Apply now in a few quick clicks

By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.