Pharmacovigilance Processes Project Manager

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Job description

* Pharmacovigilance Processes Project Manager - Pharma - contract - Remote UK *

My client is a Global Biopharmaceutical company and they have a position available for a Pharmacovigilance Processes Project Manager to join their team on a contract. This role can be remote, but you must be based in the UK.

As the Pharmacovigilance Processes Project Manager, you will lead and drive continuous improvement projects relevant to the scope of the QPPV function.

* Developing standardised best practice, templates, authoring instructions and guidance for production of Patient Safety outputs.
* Promoting and ensuring Patient Safety outputs are produced in accordance with High Performance Authoring (HPA) principles.
* Implementation of standards and skills with Patient Safety Therapeutic Area teams and individuals in close collaboration with Process Area Leads and Process Owners.
* Ensuring the adoption of standards and skills by developing and providing process competence and capability build training to functional groups within Patient Safety.
* Providing specialist knowledge and support to be recognized as experts and source of reference for safety teams and other stakeholders.
* Developing and maintaining framework(s) for content quality measurement and oversight.
* Assessing the effectiveness of initiatives with identification of subsequent further improvement actions as needed.
* Contribution to the definition and assessment of measurable objectives and delivery targets.
* Upon request participate and\/or support activities for GVP audits\/inspections

In order to apply for the Pharmacovigilance Processes Project Manager, contract you will possess a Life sciences degree and formalised training and hands-on project management experience so as to take ownership for day-to-day planning, development and managing execution of the project (both interim tool development and process build). You will be IT savvy, Excel superuser and have advanced knowledge of SharePoint applications. Solid pharmacovigilance experience, especially within (EU) health authority Assessment Reports to Periodic Safety Reports is a must.

Before you apply for this position it is vital that you are in possession of an EU or UK passport or relevant visa to work without restrictions in the UK.

To apply for this position or if you want to discuss other roles that we are working on, please do not hesitate to contact Roberta Atkins on