Global Clinical Operations- Clinical Project Manager

Novartis UK

United Kingdom
On-site
Day-to-day planning, executing and reporting
Single point of contact and study team lead
Aligned communication with trial lead
Novartis UK is seeking a Global Clinical Operations Clinical Project Manager responsible for overseeing the planning, execution, and reporting of Global Drug Development studies. The ideal candidate will have extensive experience in clinical research and project management, with strong leadership and communication skills, specifically in a matrix environment

Job Summary

  • The SSO Clinical Project Manager (CPM) is accountable for the day-to-day planning, executing and reporting of assigned Global Drug Development (GDD) studies in compliance with Novartis processes and regulatory requirements.
  • The CPM is the single point of contact and study team lead, within the country/cluster/hub, for the assigned studies, responsible for assuring aligned communication with Trial Lead and other CTT members.
  • Accountable for execution and reporting of assigned GDD studies, the CPM also participates in the review process of Site Monitoring Plans across Portfolio.

Matching Summary

Match Score: 85

Novartis UK is seeking a Global Clinical Operations Clinical Project Manager responsible for overseeing the planning, execution, and reporting of Global Drug Development studies. The ideal candidate will have extensive experience in clinical research and project management, with strong leadership and communication skills, specifically in a matrix environment.

Skills & Requirements

Must-have

  • day-to-day planning, executing and reporting
  • single point of contact and study team lead
  • aligned communication with Trial Lead
  • drive the conduct of the study
  • ensure recruitment targets are met
  • oversee local study team activities
  • monitoring quality and issue resolution
  • budget and contract negotiations

Nice-to-have

  • innovative solutions for site and patient participation
  • proactively identifies risk and opportunities
  • promotes a compliance culture
  • continuous improvement initiatives

Key Requirements

  • Minimum 5 years’ experience in clinical research
  • Degree in scientific or health discipline
  • Fluent in both written and spoken English
  • Capable of leading in a matrix environment

Work Rights

Not specified

Tailored Resume

Cover Letter