At a Glance
- Tasks: Support regulatory submissions and ensure compliance throughout clinical trials.
- Company: Join Medpace, a leader in clinical research with a supportive team.
- Benefits: Full-time position with competitive salary and career advancement opportunities.
- Why this job: Make a difference in clinical trials while developing your skills in a dynamic environment.
- Qualifications: Life sciences degree and two years' experience required, along with Microsoft Office proficiency.
The predicted salary is between 30000 - 40000 £ per year.
Medpace, Inc. is seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team in Stirling.
The role supports daily regulatory submissions activities, timelines, and documentation throughout the trial management process.
You will collect, review, assemble submissions, liaise with research sites, and ensure compliance with regulations.
A life sciences degree and at least two years' experience are required, with strong Microsoft Office skills and
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Regulatory Submissions Specialist — Clinical Trials in Stirling employer: Medpace, Inc.
Medpace, Inc. is an excellent employer for those seeking a dynamic role as a Feasibility Data Visualization Analyst in London. With a flexible work environment, competitive compensation, and a strong focus on structured career development, employees are empowered to grow and thrive while collaborating closely with clinical operations and medical teams to enhance data strategies. This supportive culture fosters innovation and meaningful contributions to clinical research.
