Medical Director Pharmacovigilance in London

26 Nov 2018
24 Dec 2018
Contract Type
Julia Day at CK Clinical is looking is looking to source a Consultant Safety Physician to join a global pharmaceutical company in London. Working as the Medical Director, Pharmacovigilance (Global) you will support the business in both early and late clinical development.

The Company:
A global pharmaceutical company with an excellent portfolio of medicines including oncology, cardiovascular, GI and pain.

London (central)

The Role:
· Company wide safety expert for four products (across therapies)
· Interactions with external experts and regulatory agencies and partner/co-development companies
· Responsible for development of documents and for negotiation with Regulatory authorities on safety matters
· Review and/or sign off of protocols, SAPs, clinical study reports, IBs, IMPD and other documents developed for submission to regulatory authorities
· Perform activities required to serve as Global PV physician:
· Review and oversight of safety data, both non-clinical and clinical
· Authorship and sign off of Safety Monitoring Plan/Risk Management Plan

Your Background: 
· Qualified physician (Licence, e.g. GMC registered, preferred)
· Extensive experience in pharmacovigilance
· Experience within global safety
· Knowledge of principles of epidemiology and statistics

The Benefits:
· 6 month initial contract
· Limited company daily rate
· Flexible working arrangements

Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.

CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.  Please quote reference CL43832 in all correspondence.

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