Pharmacovigilance Specialist, Case Processing

This is a fully remote position, open to applicants in United Kingdom, +3 more countries.

📋 Description

• Manage adverse event cases on a daily basis, which includes both clinical trial and/or post-marketed cases.

• Apply MedDRA coding to cases.

• Assess the seriousness and expectedness at both the event and case levels.

• Execute case follow-up activities and determine additional information to gather.

• Draft and evaluate case narratives.

• Issue client notifications as necessary for case management.

• Assist in the development of training materials and the delivery of training sessions.

• Bring attention to ICSR issues and inconsistencies to the Principal PV Specialist and/or Manager.

• Conduct peer reviews to ensure quality, consistency, and accuracy of cases.

• Undertake other duties as assigned.

⛳️ Requirements

• A Bachelor's degree in life sciences is mandatory.

• A minimum of two years of relevant work experience.

• Exceptional verbal, written, and interpersonal communication abilities.

• A high degree of accuracy and attention to detail.

• Capability to identify and address issues promptly.

• Ability to work both independently and as part of a multidisciplinary team.

• Strong organizational and prioritization skills, with an aptitude for multitasking.

• Basic understanding of Pharmacovigilance.

• Current knowledge of global safety regulations related to pharmaceuticals.

• Preferred qualifications include an advanced degree, RN, RPh, PharmD, or equivalent.

🏝️ Benefits

• Support for remote working options.

• Hybrid work arrangements are encouraged for new hires who are within a reasonable commuting distance from an office, as discussed with the manager.

• A workplace that is an Equal Opportunity Employer, dedicated to diversity, equity, and inclusion.