Clinical Safety Coordinator

Medpace, Inc.; Stirling; On-site; GBP 30,000 - 42,000; Full time

Job summary

Medpace, Inc. in Stirling, Scotland, is seeking a full-time Clinical Safety Coordinator to join our pharmacovigilance team.

The role focuses on distributing safety reports, maintaining trackers, and ensuring timely notifications while collaborating with Clinical Operations and Regulatory Submissions teams. Ideal candidates have a Bachelor of Science and at least 1 year of clinical trial safety experience, with strong attention to detail and working knowledge of GCP guidelines.

Qualifications

• Educated to degree level, Bachelor of Science; relevant clinical safety training preferred
• 1+ years clinical trial safety experience
• Demonstrate strong attention to detail and accuracy
• Familiarity with Good Clinical Practice (GCP) guidelines is advantageous
• Knowledge of Electronic Data Capture (EDC) systems preferred

Responsibilities

• Distribute safety reports to regulatory authorities
• Create and maintain project trackers and status reports
• Distribute and track safety-related notifications
• Perform quality control reviews of departmental documents
• Coordinate with Clinical Operations, Data Management and Regulatory Submissions

Skills

Attention to detail

Clinical safety experience

GCP knowledge

Education

Bachelor of Science

Tools

Microsoft Office

Job description

Job Summary

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, not mandatory);
• Knowledge of Electronic Data Capture (EDC) systems and other clinical databases (preferred, not mandatory);
• Knowledge of applicable safety reporting guidelines (preferred, not mandatory).