Snr. Associate, Regulatory Project Management

Looking to further your career? An amazing opportunity has arisen for a Snr. Associate, Regulatory Project Manager in Cambridge. This role is dedicated to overseeing all regulatory functions across theb organisation.

Job Responsibilities

• Updating and managing the MS Project file for the launch of the Gilead Development PMO
• Managing the Development PMO Change Management plan
• Preparing and maintaining templates and tools with the MS Project suite of apps
• Preparing training materials
• Optimising slide decks for PMO leads to deliver impactful presentations
• Maintaining the PMO glossary
• Maintaining the MS Teams team page
• Maintaining customer focussed media such as SharePoint or MS Project
• Helping design a project repository to enable dashboard reporting for 2 levels of governance (Initiative and Project)
  
  

Skills and Requirements

• Strong MS Project skills
• Advanced level MS Office skills
• Strong technical ability with project repositories
  Minimum of 3 years PMO experience.
• Experience of collaborating using Zoom, Skype for Business, or similar, with colleagues in other countries, particularly where English is not their first language.
• An understanding of pharmaceutical regulatory processes, manufacturing, change control and global distribution systems is an advantage.
  

To Apply

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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