At a Glance
- Tasks: Lead global regulatory submissions and manage essential documents for clinical trials.
- Company: Join Medpace, a leader in clinical research with a supportive team culture.
- Benefits: Full-time role with competitive salary and opportunities for professional growth.
- Other info: Office-based role with a dynamic team focused on innovation.
- Why this job: Make a difference in clinical trials while developing your leadership skills.
- Qualifications: Extensive clinical research experience and strong communication skills required.
The predicted salary is between 56700 - 69300 £ per year.
Medpace, Inc. in the United Kingdom is seeking a Regulatory Submissions Manager to join our Clinical Operations team on a full-time, office-based basis. You will oversee global start-up activities and manage submission documents to support trial execution.
Ideal candidates have:
- Extensive clinical research experience (preferably with a CRO)
- Knowledge of Clinical Trial Applications in Europe
- Strong oral and written communication skills
- A collaborative, leadership-driven approach
Global Regulatory Submissions Lead for Clinical Trials employer: Medpace
Medpace is an exceptional employer, offering a collaborative and purpose-driven work environment in Cincinnati, Ohio, where employees can thrive alongside industry-leading experts in clinical research. With a strong focus on continuous learning and professional development, Medpace provides defined career paths, comprehensive benefits, and a culture that encourages innovation and employee contributions. Join us to make a meaningful impact on global health while enjoying competitive compensation and a supportive office-based atmosphere.
