MSI Pharma is partnering with one of the largest and diversified healthcare organizations in the world on a Regulatory Data (XEVMPD) role on an initial 12-month contract - with the possibility of extension.

This is a global role supporting data needs in the EU, US and the Rest of the World; with a key focus on providing support for the Product and Lifecycle Registration (PLcR) capability, based on the InSight for Registrations software platform.

The ideal candidate should display the ability to prioritise work, collaborate with regional teams and users, as well as demonstrate the ability to work independently in a virtual environment.

Key Knowledge/Skills/Experience Required:

- Ability to work effectively as part of a virtual team of regulatory data experts operating in a matrix-managed and international environment

- Knowledge of regulatory business processes; 3 to 5 years' experience preferred

- Knowledge of and experience with XEVMPD submissions essential

- Experience of working with InSight for Registrations highly desirable

Start date: Mid-September / October

This role is remote with occasional visit to the office - based in High Wycombe, UK.

Full job specification(s) available upon request.

If you are interested, then please apply now! If you would like more information, then email me or call (phone number removed)