Snr. Associate, Regulatory Project Management

Highly Competitive
  1. Permanent
  2. Project Manager
  3. United Kingdom
Cambridge, England
Posting date: 21 Sep 2020

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.