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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