Entry Level Life Science Jobs at Medpace
Medpace is hiring an Entry Level Regulatory Submissions Coordinator to join its growing Clinical Operations team in Stirling, United Kingdom. This is a full-time, office-based graduate role. The Life Science Jobs at Medpace offer an excellent opportunity for life sciences graduates who are interested in clinical trials and regulatory processes and want to build a long-term career within a global Contract Research Organization (CRO).
Job Details:
- Job Title: Entry Level Regulatory Submissions Coordinator
- Location: Stirling, United Kingdom
- Department: Site Activation & Maintenance / Clinical Operations
- Job ID: 12536
- Employment Type: Full-time
- Work Model: Office-based
About the Company:
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. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 professionals across 40+ countries and supports clinical research across multiple therapeutic areas, including oncology, cardiology, metabolic disease, CNS, and infectious diseases.
Educational Requirements for the Regulatory Submissions Coordinator Role:
- Bachelor’s degree in a Life Sciences field
Key Responsibilities:
- In the Life Science Jobs at Medpace, you should provide day-to-day departmental support to Regulatory Submissions Coordinators
- Maintain databases and spreadsheets to track regulatory and departmental activities
- Collect, review, organize, and assemble regulatory start-up submissions
- Prepare, review, and file clinical trial applications in the Regulatory Submissions Coordinator Role
- Communicate with research sites, such as hospitals, to collect essential regulatory documents prior to site activation in the Life Science Jobs in the UK.
- Ensure regulatory submissions comply with applicable regulations and guidance documents
- Maintain timelines for study start-up through internal and external collaboration
- Provide input on regulatory submission documents in the Life Science Jobs
- Perform additional administrative and regulatory tasks as required
Skills Required for Life Science Jobs:
- Strong interest in clinical trials and regulatory processes
- Knowledge of Microsoft Office applications
- Excellent organizational and communication skills
- cCose attention to detail
- Ability to manage documentation and timelines effectively
- Strong collaboration and coordination abilities
Benefits of the Regulatory Submissions Coordinator Role:
- Flexible work environment
- Competitive compensation and benefits package
- Competitive paid time off (PTO)
- Structured career paths with clear professional growth opportunities
- Employee appreciation events sponsored by the company
- Employee health and wellness initiatives
- Opportunity to work with a globally recognized CRO
- Contribution to clinical research that improves patient lives worldwide
