Senior Pharmacovigilance Associate

PrimeVigilance

Lisbon or Remote, Portugal

Job Description

At PrimeVigilance, Senior PV Associates are experienced case processing team members who are expected to manage a variety of case processing services with minimal guidance from senior team members.

If you join PrimeVigilance, you can expect to work with teams of different sizes, from small clinical trial, to large, generic post-marketing teams. We are always looking for proactive, capable and motivated individuals who aim to surpass any target set in front of them. Senior PV Associates are expected to reach and maintain a high level of performance within 5 months of being assigned to an ICSR team, following onboarding completion.

Responsibilities include:

Processing of Individual Case Safety Reports from all sources (post-marketing and clinical trials) in compliance with applicable regulations, PrimeVigilance procedures and in accordance with client specific requirements and timelines, focusing on triage, data entry, quality review and submissions workflow steps
Reconciliation activities for all types of received reports
Workflow management activities

Qualifications

We expect:

Life science/bio medical background – healthcare related degree (chemistry, biology, biotechnology, veterinary science) and demonstrated experience in Pharmacovigilance case processing
ARGUS experience preferred
Time and issue management, delegation, organization and multitasking skills with good attention to detail
Strong interpersonal and communication skills
Fluency in English skills, both verbal and written, at least B2

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