At a Glance
- Tasks: Support regulatory activities and ensure timely submissions for research studies.
- Company: Medpace, a leader in clinical research with a focus on growth and flexibility.
- Benefits: Flexible work environment, competitive salary, and opportunities for professional development.
- Other info: Great opportunity for career advancement in a supportive environment.
- Why this job: Join a dynamic team and contribute to impactful research in the life sciences.
- Qualifications: Life Sciences degree and 2+ years of experience in regulatory submissions.
The predicted salary is between 30000 - 40000 £ per year.
Medpace is seeking a Regulatory Submissions Coordinator to support day-to-day regulatory activities and ensure timely start-up submissions.
You will maintain databases and collaborate with research sites to collect essential documents, supporting timelines from start-up through to study enrollment.
The role requires a Life Sciences degree, 2+ years of experience in regulatory submissions, and strong organization and communication skills.
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Regulatory Submissions Specialist - Flexible & Growth-Oriented in Stirling 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.
