Clinical Safety Coordinator

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

Our Safety activities are growing rapidly, and we are currently seeking a full‑time, Clinical Safety Coordinator to join our team in Stirling, Scotland. This position plays a key role in the pharmacovigilance process at Medpace, working in a team to accomplish tasks and projects that are instrumental to the company’s success.

If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

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.

Qualifications

• Educated to degree level, Bachelor of Science.
• 1+ years clinical trial safety experience.
• Strong attention to detail.
• Comprehensive understanding of Microsoft Office suite.
• Demonstrate fundamental knowledge of Good Clinical Practice (GCP) guidelines and medical terminology (preferred, but not mandatory).
• Knowledge of Electronic Data Capture (EDC) systems and other clinical databases (preferred, but not mandatory).
• Knowledge of applicable safety reporting guidelines (preferred, but not mandatory).

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

What To Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.