At a Glance
- Tasks: Lead global regulatory submissions and ensure high-quality documentation.
- Company: Join Medpace, a leader in clinical operations with a collaborative culture.
- Benefits: Enjoy a supportive office environment with growth opportunities and competitive pay.
- Other info: Dynamic team atmosphere with ongoing professional development.
- Why this job: Make a real impact in clinical research while developing your leadership skills.
- Qualifications: Extensive clinical research experience and strong regulatory knowledge required.
The predicted salary is between 59400 - 72600 £ per year.
Medpace is seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team.
The role focuses on managing global start-up, ensuring high-quality submission documents, and presenting at audits and defenses.
The position requires extensive clinical research experience, regulatory knowledge in Europe, and strong communication and leadership abilities.
An office-based, collaborative environment with ongoing growth opportunities is offered.
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Global Regulatory Submissions Lead 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.
