Pharmacovigilance Case Processing Specialist

ProPharma; Stockholms kommun; On-site; SEK 420,000 - 540,000; Full time

Job summary

ProPharma is seeking a Pharmacovigilance Specialist, Case Processing, to manage individual case safety reports and assess seriousness and expectedness, ensuring timely regulatory submissions. You will create narratives, perform follow-ups, and work with clients to maintain high-quality safety data, while keeping up with global regulations.

A life sciences degree and at least two years’ related experience are required.

Qualifications

• Bachelor’s degree in life sciences required.
• Two years of related work experience.
• Fluency in English and Swedish.
• Basic knowledge of pharmacovigilance.
• Strong communication and multitasking abilities.

Responsibilities

• Daily case processing of adverse event cases, including coding with MedDRA.
• Follow-up activities to obtain missing information.
• Create and review case narratives.
• Provide client notifications for case management.
• Assist in training materials and delivery.
• Identify discrepancies and escalate to supervisors.
• Stay updated on global safety regulations.
• Peer reviews for quality and accuracy.
• Other duties as assigned.

Skills

English & Swedish

Communication

Attention to detail

Problem solving

Teamwork

Organization

Pharmacovigilance basics

Education

Bachelor's in life sciences

Advanced degree (RN/PharmD)

Job description

ProPharma is seeking a Pharmacovigilance Specialist, Case Processing, to manage individual case safety reports and assess seriousness and expectedness, ensuring timely regulatory submissions. You will create narratives, perform follow-ups, and work with clients to maintain high-quality safety data, while keeping up with global regulations.

A life sciences degree and at least two years’ related experience are required.