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Regulatory Affairs Project Manager

BerkshireTemporary
£65 - £70 per hour
Job Reference: J5635746
Updated On: 24/11/2021
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Biotechnology

Skills: Regulatory Affairs - Contract, Regulatory Affairs - Global, Regulatory Affairs - Operations, Regulatory Affairs - Biologics

Job Information

Role Overview

We are currently looking for a Regulatory Affairs Project Manager to join a leading Pharmaceutical company based in the Berkshire area. As the Regulatory Affairs Project Manager you will be responsible for overseeing relationships with vendors to ensure Regulatory Service Agreements are supporting business needs. This is a 12 month contract with possibility of an extension or permanent offer thereafter.

Key Duties and Responsibilities

Your duties as the Regulatory Affairs Project Manager will be varied however the key duties and responsibilities are as follows:

1. Drive Regulatory Service Agreements (RSA) with vendors and stakeholders to ensure agreed deliverables are achieved/met.

2. The Regulatory Affairs Project Manager will work within a Global Regulatory and matrix environment.

3. The Regulatory Affairs Project Manager should possess experience with Regulatory content management systems / document management systems (EDMS/ECMS/Veeva).

4. Able to project manage, conduct negotiations with vendors and work autonomously.

Role Requirements

To be successful in your application to this exciting opportunity as the Regulatory Affairs Project Manager we are looking to identify the following on your profile and past history:

1. Relevant degree in a Pharmaceutical or Biologics based discipline.

2. Proven industry experience in a Global Regulatory Affairs and/or matrix working environment. Previous experience working for a CRO is an advantage.

3. A working knowledge and practical experience with project managing Regulatory Service Agreements and content management systems implementation.


Key Words: Regulatory Affairs Project Manager / RA / Regulatory Affairs / Veeva / Regulatory Information Management / RIM / EDMS / ECMS / Regulatory Content Management / Pharmaceutical / Biotechnology / Biologics / RSA / Regulatory Service Agreement / Global Regulatory Affairs / CRO / Contract Research Organisation
Fabio Roque
Your Recruitment ConsultantFabio Roquefabio.roque@hyperec.com
DisclaimerHyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.