Full-Time Senior PV Officer
Ergomed is hiring a remote Full-Time Senior PV Officer. The career level for this job opening is Senior Manager and is accepting Mississauga, Canada based applicants remotely. Read complete job description before applying.
Ergomed
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Assures and exerts of activities leading to effective cooperation with clients in the area of ICSR Management.
Contributes to achieving company's goals and objectives.
Works independently.
Clinical case processing
- Providing support to other activities undertaken by the project team on behalf of the client and the company.
- Performing activities in the scope of ICSR management unit within agreed extent and timeframe (including, but not limited to):
- Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations, PrimeVigilance procedures and in accordance with client specific requirements and timelines.
- Performing ICSR follow up.
- SAE/SUSAR Management (unblinding, clinical trial reconciliation, protocol review, Safety Management Plan review).
- Reconciliation (clinical, partners).
- Personal data protection.
- Product Quality Complaint handling and interaction with Quality Assurance.
- Medical Information interaction.
- MedDRA and WHO coding.
- Database Outputs and Reports (including data for monthly reporting to clients).
Workflow & resource management.
Mentoring and training of new and more junior employees within the department.
Support of PV processes related to the ICSR management within PrimeVigilance and also to clients.
Supporting ICSR SMEs or contributing as one of ICSR SMEs.
More senior colleague may perform tasks assigned as per SOP to more junior position.
Performing activities in the scope of ICSR management unit within agreed extent and timeframe.
Supporting the RA & PV Network Department as needed, including acting as the LCPPV (Local Contact Person for Pharmacovigilance) for the specified country and taking on the role of PRLS (Person Responsible for Local Screening) for the designated language, as agreed with the line manager.
Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance
3-4 years of work experience in pharmacovigilance including clinical
Excellent communication (written and verbal) skills
Organization skills, including attention to details and multitasking
Delegation skills
Planning and time management
Technical skills
Team working
English – fluent (spoken, written)
Advanced literacy (MS Office)