Clinical Safety & Pharmacovigilance Specialist

Medpace; Stirling; On-site; GBP 35,000 - 55,000; Full time

Benefits offered by this job

Health benefits

On-site training

WFH after training

Job summary

Medpace, Inc. in Stirling is seeking a Clinical Safety professional to join our European Pharmacovigilance team.

You will collect, process and track SAE reports, generate safety narratives, and contribute to safety data entry and QC within a fast-paced, cross-functional environment. Working alongside medical monitors and QA, you will support safety documentation, lead safety projects, and participate in sponsor meetings.

Qualifications

• Bachelor’s degree in life sciences.
• 2+ years of Clinical Trial Pharmacovigilance experience.
• Familiarity with safety databases; Argus is desirable.
• Strong medical terminology and GCP knowledge.
• Experience on global trials as part of multi-disciplinary teams.

Responsibilities

• Collect, process, and track SAE reports.
• Generate safety narratives and safety queries.
• Safety database data entry and QC of safety cases.
• Prepare Investigator Safety Letters and SAE reconciliations.
• Lead clinical safety projects and attend sponsor meetings.

Skills

SAE reporting

Safety narratives

Data entry

Quality review

Education

Bachelor’s life science degree

Tools

Safety databases (Argus)

Job description

Medpace, Inc. in Stirling is seeking a Clinical Safety professional to join our European Pharmacovigilance team.

You will collect, process and track SAE reports, generate safety narratives, and contribute to safety data entry and QC within a fast-paced, cross-functional environment. Working alongside medical monitors and QA, you will support safety documentation, lead safety projects, and participate in sponsor meetings.