Position Overview & Specifications

Significant experience in directing complex programs within the pharma industry
Permanent position
Work for a Global company!

PROJECT MANAGER | PHARMACEUTICAL
PERMANENT

UK – Remote
£50k - £60k + up to 20% annual bonus
Private healthcare + other excellent benefits!

THE ROLE…

Leading and driving a series of key Research & Development / Life cycle Management programmes supporting our client to enable product development, security of supply and to support clinical and commercial products as required
Accountable for building and driving key programs to fruition. As part of this will manage project plans, co-ordination of meetings with internal and external stakeholders and ensure that all project related action items are closed on time and to a high standard. Have a clear understanding of the project requirements and all activities for delivery and provide regular updates to Senior Management.
Interface with external third parties to ensure full and proper coordination of activities required for a new product launch.
Conduct troubleshooting activities for projects and escalate key issues and updates in a timely fashion. Work with a cross-functional team to ensure successful provision of R&D /LCM programmes on time and to the required quality.
Identify and map potential new R&D, medical and clinical programmes required, build Business Cases to pitch and initiate programmes.
Secure appropriate sponsorship via senior management based on a review of cost, benefit, risks and timelines within the broader business.
Ensure that the operational side of the Programme Management is fully optimised in support of future business plans including ensuring processes are in place and functional.

WHAT YOU WILL NEED..

Degree in an appropriate scientific discipline.
Project Management Qualification, e.g. Prince2, PMP etc.
Significant experience in directing complex programs within the pharmaceutical/biopharmaceutical sector (>10 years).
Subject-matter expert in a biological/pharmaceutical discipline
Understanding and hands–on working knowledge of cGxP, quality, clinical, regulatory and manufacturing requirements for commercial material

BENEFITS...