Employer Active
Job Alert
You will be updated with latest job alerts via emailJob Alert
You will be updated with latest job alerts via emailThe Senior Pharmacovigilance (PV) Physician II is responsible for medical review of ICSRs writing and reviewing signal detection reports writing and/or reviewing aggregate reports (DSURS PSURS/PBRERs/PADERS ACOs responses to regulatory authority requests) writing and/or reviewing riskmanagement reports (RMPs) and mentoring junior PV Physicians. The Senior PV Physician II is also expected to support the QPPV in medical aspects and safety issues as may be required by Company or Client.
For the Client :
To review and approve postmarketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports for medical/causality assessment. Review includes coding assessment of seriousness listedness/expectedness and Company causality as well as writing of Company comment followup questions and Analysis of Similar Events when required. Including completion of all required supporting documentation such as trackers.
To complete the adverse event tracker for all ICSRs reports
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 approve 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/to lead the preparation of responses to regulatory authority requests
Can act as EEA QPPV and/or Deputy for up to 2 clients if required.
To review and provide input in Periodic Safety Update Reports Development Safety Update Reports ACOs or Annual Safety Reports.
To act as Company Lead in a specific pharmacovigilance area requiring medical input (e.g. for preparation of reference safety information Company Core Data Sheet)
Actively participate in the Drug Safety Review Committee signal detection and risk evaluation process for Client company medicinal products in the products life cycle.
Serves on Clients advisory and scientific committees.
Signalling
Reviewing line listings
Participating in signal detection activities including meetings reviewing of signal detection reports and providing consultation to clients on aspects related to benefit/risk assessment and risk minimisation
Evaluating and categorizing possible signals
Proposing a course of action whenever a possible signal is identified
Supporting preparation and review of benefitrisk reports
Supporting PV Project Managers in the planning of signalling schedule and resources
Supporting PV Project Managers in the preparation of projectspecific working instructions regarding signalling
Overseeing the quality of signal detection activities and providing quality and compliance metrics to the Quality Department
For the Company
To support the preparation of PV procedures
To provide training and mentoring of junior PV Physicians
To provide medical advice and input to project teams on daily basis
Training mentoring and managing junior PV Physicians
Continuously working on the development of the procedures on the company level
Preparing or contributing to the preparation of signalling related company procedures
The Senior PV Physician will support the Director of Projects as well as the QPPV on a day to day basis as needed
Supporting the Medical Director in training and mentoring on signalling activities
Qualifications :
The PV Physician should be medically qualified as a physician with demonstrated experience in PharmacoVigilance and working in a clinical setting.
Endocrinology experience is required.
Excellent interpersonal skills
Ability to plan organise prioritise and execute multiple tasks
Ability to work effectively cross culturally and cross functionally and value the importance of teamwork
Communication skills
Presentation skills
Remote Work :
Yes
Employment Type :
Fulltime
Remote