To review and approve postmarketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding seriousness assessment Company causality and comment listedness/expectedness and followup questions.
To act as a Qualified Person for Pharmacovigilance or support the Qualified Person for Pharmacovigilance (if not medically qualified) in the medical understanding and evaluation of any safety issues
To review and provide input in Periodic Safety Update Reports Development Safety Update Reports literature screening search strategy
To review articles to determine if they contain ICSRs/SAEs related to the relevant Medicinal Product or other safety related findings
To cooperate in the preparation of and provide input in Risk Management Plans
Supporting the preparation of responses to regulatory authority requests
Signalling
Reviewing line listings
Participating in signal detection activities including meetings writing signal detection reports if applicable if required and providing consultation to clients on aspects related to benefit/risk assessment and risk minimisation
Evaluating and categorizing possible signals and proposing a course of action
Supporting preparation and review of benefitrisk reports
Qualifications :
The PV Physician should be medically qualified as a physician
Previous experience in pharmacovigilance
Ability to review different aggregate report types including PBRERs and DSURs
Expertise in signal detection activities is essential
Excellent interpersonal skills
Ability to plan organise prioritise and execute multiple tasks
Ability to work effectively crossculturally and crossfunctionally and value the importance of teamwork
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