Pharmacovigilance Case Processing Specialist

ProPharma Group; Sweden; Hybrid; SEK 480,000 - 640,000; Full time

Job summary

ProPharma Group is seeking a Pharmacovigilance Specialist, Case Processing, to manage adverse event cases, code with MedDRA, and prepare medical narratives. You will perform follow-ups, assist with regulatory reporting, and maintain regulatory knowledge as part of a cross-functional PV team.

The role offers hybrid work with opportunities for collaboration across client projects and regional teams. A life sciences degree with PV experience is required or preferred depending on the context.

Qualifications

• Bachelor's degree in life sciences required.
• Two years of PV or related experience preferred.
• Strong verbal and written communication with high attention to detail.
• Ability to work independently and in a multidisciplinary team.

Responsibilities

• Process daily adverse event cases, including coding using MedDRA.
• Perform follow-up to obtain missing or unclear information.
• Create and review medical narratives for accuracy.
• Provide client notifications as required for case management.
• Maintain up-to-date knowledge of global safety regulations.
• Peer review cases for quality, consistency and accuracy.

Skills

Verbal communication

Written communication

Attention to detail

Problem solving

Multitasking

Organization

Team collaboration

Pharmacovigilance

Education

Bachelor's degree in life sciences

Advanced degree in life sciences

Tools

MedDRA

Job description

ProPharma Group is seeking a Pharmacovigilance Specialist, Case Processing, to manage adverse event cases, code with MedDRA, and prepare medical narratives. You will perform follow-ups, assist with regulatory reporting, and maintain regulatory knowledge as part of a cross-functional PV team.

The role offers hybrid work with opportunities for collaboration across client projects and regional teams. A life sciences degree with PV experience is required or preferred depending on the context.