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Pharmacovigilance Physician

Pharmacovigilance Physician
Type: Permanent
Salary: Flexible depending on experience
Location: Home counties

Our client is a global company providing clients with expert advice at all stages of the drug development process. They offer a range of services including consulting, development, regulatory and pharmacovigilance management. The main purpose of the role is to provide pharmacovigilance expertise and advice on medical safety aspects of client projects.

Main Duties

* To ensure all post marketing pharmacovigilance work conducted or planned has adequate safeguards with regard to patient safety and is ethical.
* To work with and on behalf of Project teams to overview and assess adverse events and adverse event patterns
* To provide medical oversight of post marketing pharmacovigilance services. To assist in providing medical oversight in pre-approval and peri-approval pharmacovigilance services
* To provide medical review and writing support (case narratives, PSURs, ASRs)
* To represent the company at client meetings where medical/pharmacovigilance issues need to be discussed
* To be the designated signatory, if appropriate, where this is required by a medically qualified person
* To act as a QPPV/deputy QPPV on behalf of clients, if required
* Where necessary to provide strategic input into clinical development programmes

Requirements

* Relevant Medical qualifications (to include at least one higher medical qualification), significant and recent direct medical experience
* Expertise in pharmacovigilance processes and associated medical issues (minimum 5 years) including PSURs, literature search review and AE management
* Knowledge of medical monitoring
* Therapeutic knowledge to provide input into project design, proposal development and bid preparation in a range of therapeutic areas:
* Computer literate/ effective use of available technology

For more information or to apply please email peter@clinicalprofessionals.co.uk or call 0118 959 4990

Key words: Periodic safety update reports safety signal detection clinical pharmaceutical biotechnology medical devices CRO clinical trials clinical development pharmacology health medical research drug safety pharmacovigilance adverse event reporting aris g Arisg PSUR adverse event case processing ADR data physician GMC QP narrative Argus SAE reconciliation safety PV DS PVG PVO SUSARs SARs GMC

We are dedicated to the clinical research industry, offering candidates a unique service including our free \"Pipeline Watch\" career advisory consultation. To find out more call us on 0118 9594990 or email apply@clinicalprofessionals.co.uk