At a Glance
- Tasks: Coordinate safety reports and collaborate with global teams to ensure clinical excellence.
- Company: Join Medpace, a leading clinical research organisation making a real impact in healthcare.
- Benefits: Competitive pay, health perks, flexible work options, and career growth opportunities.
- Other info: Dynamic workplace with mentorship and continuous learning to boost your career.
- Why this job: Be part of a mission-driven team advancing medical therapies and improving patient outcomes.
- Qualifications: Degree in science and some experience in clinical trial safety preferred.
The predicted salary is between 51750 - 63250 £ per year.
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 I-IV 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. Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
Clinical Safety Coordinator employer: Medpace
Join our dynamic Clinical Operations team in London, where we prioritise employee growth and foster a collaborative work culture. As a Clinical Trial Site Relationship Coordinator, you'll benefit from ongoing professional development opportunities while working in a vibrant environment that values strategic relationships and innovative solutions in clinical research. Enjoy the unique advantage of reduced travel while making a meaningful impact in the field of clinical trials.
