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    • 1+ years clinical trial safety experience.
    • Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development…
    • View all Medpace, Inc. jobs - Stirling jobs - Safety Coordinator jobs in Stirling
    • Salary Search: Clinical Safety Coordinator salaries in Stirling
    • See popular questions & answers about Medpace, Inc.
    • Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to…
    • Develop methods and improvement of the planning and execution of clinical studies.
    • Eurofins Scientific is an international life sciences company, providing a…
    • SGS’s Life Sciences services support the pharmaceutical, biotech, and healthcare sectors with expert testing, clinical research, auditing, and certification—…
    • Salary Range: £37,694 - £46,049.
    • FTE: 1 (35 hours/week).
    • Contract Type: Fixed (24 months).
    • Closing Date: 25/08/26.
    • Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to…
    • Ross Hall Hospital, Glasgow, Scotland.
    • Up to £71,150 per annum DOE.
    • Location: Ross Hall Hospital, Glasgow, G52 3NQ.
    • Contract /Hours: Permanent/37.5 per week.
    • Knowledge of Parkinson's disease biology, biomarker development or clinical research would be advantageous.
    • The postholder will bring together sample processing…
    • Bachelor’s degree in microbiology, biology, biochemistry, chemical engineering, or related discipline (Master’s Degree is preferred).
    • Be the First to Apply.
    • Be the First to Apply.
    • Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and…
    • Quality Control Analyst I – Microbiology.
    • Location: Edinburgh BioQuarter, Little France.
    • We are RoslinCT, a world-leading cell and gene therapy contract…
    • As Study Manager, you will be responsible for leading customer studies from initiation through to completion, ensuring that scientific objectives, timelines,…
    • HCPC registration or IBMS membership is preferred (or equivalent clinical laboratory experience).
    • Previous hands-on experience with Next Generation Sequencing (…
    • HCPC registration or IBMS membership is preferred (or equivalent clinical laboratory experience).
    • Previous experience in a molecular biology, clinical…
    • Prior sales/clinical support experience preferred.
    • Ability to be an integral part of an innovative, fast paced clinical & business development team.

Job Post Details

Clinical Safety Coordinator - job post

Medpace, Inc.
2.6 out of 5 stars
Wallace House 17-21 Maxwell Place, Stirling FK8 1JU
Full-time
You must create an Indeed account before continuing to the company website to apply

Job details

Job type

  • Full-time

Location

Wallace House 17-21 Maxwell Place, Stirling FK8 1JU

Benefits

Pulled from the full job description

  • Annual leave
  • Work from home
  • Company events

Full 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).
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

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.
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