Clinical Safety Coordinator

Medpace; United States; Remote; USD 43,000 - 56,000; Full time

Benefits offered by this job

On-site mentors

Defined career paths

Industry onboarding and training

Ongoing professional development

Competitive compensation

Comprehensive health and retirement

Occasional WFH after training

Company-sponsored social events

Job summary

Medpace is seeking a full-time Clinical Safety Coordinator in London to support pharmacovigilance processes. You will work with a cross-functional team to distribute safety reports, maintain trackers, and ensure timely safety communications with regulators.

The role requires a Bachelor of Science and 1+ year(s) of clinical trial safety experience, with strong attention to detail and good knowledge of GCP, EDC systems, and Microsoft Office.

Qualifications

• Educated to degree level, Bachelor of Science.
• 1+ years clinical trial safety experience.
• Strong attention to detail.
• Proficient with Microsoft Office suite.
• GCP guidelines and medical terminology knowledge preferred.
• Knowledge of EDC systems and other clinical databases preferred.
• Knowledge of 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 globally.
• Perform other tasks as needed.

Skills

Attention to detail

Microsoft Office

GCP knowledge

EDC systems knowledge

Pharmacovigilance experience

Education

Bachelor of Science

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.,

• 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.
  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 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, Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace's mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 6,500 people across 46 countries.
  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