Clinical Safety Coordinator

Medpace; City Of London; On-site; GBP 36,000 - 56,000; Full time

Benefits offered by this job

Office based environment with on-site

On-site mentorship and training

Occasional WFH after training

Company-sponsored social events

Comprehensive health, retirement, and

Job summary

Medpace in London is seeking a full-time Clinical Safety Coordinator to support pharmacovigilance activities. The role involves distributing safety reports to regulators, maintaining trackers, and ensuring quality control across safety documentation.

You will work with Clinical Operations, Data Management and Regulatory Submissions to ensure compliant safety processes, with opportunities for professional growth within the Medpace global network.

Qualifications

• Bachelor of Science degree or equivalent.
• 1+ years clinical trial safety experience.
• Strong attention to detail.
• Familiarity with GCP guidelines (preferred).
• Knowledge of EDC systems (preferred).
• Understanding safety reporting guidelines (preferred).

Responsibilities

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

Skills

Attention to detail

MS Office proficiency

GCP knowledge

EDC systems knowledge

Safety reporting guidelines knowledge

Team collaboration

Education

Bachelor of Science

Tools

Electronic Data Capture (EDC) systems

Microsoft Office Suite

Job description

Our Safety activities are growing rapidly, and we are currently seeking a full-time, Clinical Safety Coordinator to join our team in London. 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).

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

• Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

• Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
• Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

• Office based environment with on-site mentors
• Defined career paths with clear advancement opportunities
• Industry renowned onboarding and training programs designed to accelerate professional development
• Ongoing training and continuous learning opportunities throughout your career
• An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

• Competitive compensation programs that recognize and reward performance
• Comprehensive health, wellness, retirement, and PTO benefits
• Office based culture with occasional WFH that provides flexibility for eligible positions after training
• Company-sponsored social events