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Job Details

Belgium, Brussels *** Drug Safety Specialist *** Safety Case Processing *** CONTRACT ROLE

Company: Advanced S&S (Medical / Clinical)
Location: Belgium, Brussels
Reference: ODADV /10350
Closing Date: 29 Apr 18
Type: Contract
Salary (£): On Application
Benefits: On Application

Job Summary:

If you wish to apply for this role, please send your CV with a covering note to oli.dimitrov@advregulatory.com or alternatively, to have a confidential discussion about this or other potential roles or career options, call Oli in the London office on +44 (0)20 7801 3380

Requirements:

Belgium, Brussels *** Drug Safety Specialist *** Safety Case Processing *** CONTRACT ROLE

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We have an urgent requirement for someone who has a strong background in Safety Case Processing. This is an opportunity for a Drug Safety Specialist for a 3-month contract role with the possibility of an extension or a permanent position. Our client is a large Pharmaceutical company based in Brussels that is expanding their global presence and developing a new hub for Drug Safety. 

You will need to have at least 5 years of experience in the pharmaceutical industry with experience in PV department or a clinically-oriented discipline, including experience in the conduct of clinical studies and/or experience in safety case processing. You need to have thorough and expert knowledge of safety systems (Argus) and how pharmacovigilance fits into the larger scope of the drug development cycle.

Main responsibilities:

•            Serves as subject matter expert on adverse event reporting and submission within patient safety and other cross functional areas.

•            Is a leader in the review and the implementation of robust communication/interfacing processes with PV outsourcing partners to ensure all outsourcing activities meet business and regulatory objectives.

•            Enhances overall ICSR system by implementing process improvements, working with other teams including but not limited to QC team, safety physicians, local safety officers, and external vendors as needed.

•            Write and maintain SOPs regarding ICSRs. Provide insight and initiate any changes needed due to changing business need, system requirements, or regulatory changes.

•            Be a point of contact for the safety case processing vendor, providing responses to queries and providing oversight on key processes.

Ideally you will speak French or Dutch and be fluent in English.

A candidate must be operational immediately - autonomous, self-starter.

______________________________________________________________________________________

If you wish to apply for this role, please send your CV with a covering note to oli.dimitrov@advregulatory.com or alternatively, to have a confidential discussion about this or other potential roles or career options, call Oli in the London office on +44 (0)20 7801 3380.

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About Advanced

Advanced Search and Selection Ltd has been operating since 2004. We are registered and licensed to recruit through the United Kingdom, mainland Europe and the Americas.

We match professional candidates to the best permanent, contract and interim roles in the market. For more information about the company visit us at www.advregulatory.com.

We provide a high level of service because we believe this matters.

Keywords / Key words: Medical, Medical Affairs, MA, Medical jobs, MA jobs, Medical Affairs jobs, Clinical Research, Clinical, Clinical jobs, Clinical Development, Project Management, Physician, Drug Safety,

To Apply : Please send a full CV in confidence to cv@advregulatory.com.

Contact Information:

Address:  Head Office
Head Office Suite 8 Penhurst House 352-356 Battersea Park Road London
SW11 3BY
England
Tel:  +44 (0)20 7801 3388
Website:  Visit Our Web Site

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