At a Glance
- Tasks: Lead proposal writing efforts to support clinical research projects and drive business growth.
- Company: Join Medpace, a global leader in clinical research with a mission to improve healthcare.
- Benefits: Enjoy competitive pay, comprehensive health benefits, and opportunities for professional development.
- Other info: Be part of a diverse team dedicated to advancing global health.
- Why this job: Make a difference in the medical field by contributing to innovative therapeutic solutions.
- Qualifications: Strong writing skills and experience in clinical research or proposal development.
The predicted salary is between 80000 - 120000 £ per year.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO).
We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.
Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach.
We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.
Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
Director of Proposal Writing in London 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.
