Clinical Safety Coordinator — Flexible Growth & Impact

Medpace; Stirling; On-site; GBP 32,000 - 45,000; Full time

Benefits offered by this job

Flexible work environment

Competitive compensation packages

Competitive PTO packages

Structured career paths with growth

Company-sponsored employee events

Employee health and wellness

Job summary

Medpace is seeking a full-time Clinical Safety Coordinator to join our Stirling, Scotland team. You will contribute to the pharmacovigilance process, distributing safety reports, maintaining trackers, and coordinating with Clinical Operations, Data Management and Regulatory Submissions to support regulatory timelines.

Ideal candidates hold a science degree and have 1+ years in clinical trial safety, with strong attention to detail and proficiency in Microsoft Office.

Qualifications

• Degree-level education, Bachelor of Science.
• 1+ years of clinical trial safety experience.
• Strong attention to detail.
• Comprehensive knowledge of Microsoft Office.
• GCP familiarity (preferred) and medical terminology (preferred).
• Knowledge of EDC systems and clinical databases (preferred).
• Knowledge of safety reporting guidelines (preferred).

Responsibilities

• Responsible for the distribution of safety reports to regulatory authorities.
• Create and maintain project-related trackers and status reports.
• Distribute and track safety-related notifications.
• Conduct quality control reviews of departmental documents.
• Regular interaction with other internal departments globally and locally, such as Clinical Operations, Data Management and Regulatory Submissions.
• Perform other tasks as needed.

Skills

Attention to detail

GCP knowledge

Medical terminology

Education

Bachelor of Science

Tools

Microsoft Office

Job description

Medpace is seeking a full-time Clinical Safety Coordinator to join our Stirling, Scotland team. You will contribute to the pharmacovigilance process, distributing safety reports, maintaining trackers, and coordinating with Clinical Operations, Data Management and Regulatory Submissions to support regulatory timelines.

Ideal candidates hold a science degree and have 1+ years in clinical trial safety, with strong attention to detail and proficiency in Microsoft Office.