My client, a top Pharmaceutical Company, has a position available for a senior Pharmacovigilance Scientist to join their team for a 12-month initial contract within their Oncology arena.
INSIDE IR35
Hybrid - 3 days London + 2 days WFH

Your new role
As the Senior Pharmacovigilance Scientist, you will support by completing delegated Pharmacovigilance tasks of scientific analyses, case reviews, data reviews & presentations, signal management and risk assessment activities, evaluation of product quality issues and emerging safety issues, including contribution to safety documents, aggregate reports, RMPs and health authority requests, submissions IND/CTA/MAA, Response to Questions (RtQ)/interactions etc. for allocated assets/products, projects and activities, including for clinical safety of assets in clinical development.

What you’ll need to succeed
In order to apply for the Senior Pharmacovigilance Scientist, you must possess:
* Bachelor’s degree in biologic or natural science or advanced degree (M.Sc., PhD, MPH, PharmD, etc.)
* Significant pharmacovigilance experience, including experience in aggregate safety reports writing, safety signal management, clinical safety and submission.
* Sound knowledge of pre- and post-marketing PV legislation including CTR and GVP Modules.
* Knowledge of product development processes and experience of cross-functional teamwork
* Knowledge of FDA/EMA or equivalent regulatory submission process
* Experience in Oncology

What you need to do now
Before you apply for this position, it is vital that you are in possession of a UK passport or relevant visa to work without restrictions in the UK and must be based 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