Responsibilities
We are currently seeking aDirector, Feasibility, who will be an integral team leader within our global Proposals and Feasibility team. This position will evaluate and support new clinical trial opportunities by working strategically with Medpace Medical Experts, Clinical Trial Managers, and our Regulatory Submissions team. By collaborating with Investigators and international country managers, as well as analysis of multiple data sources, this individual will strategize the most efficient scenario to conduct various studies globally. If you are an individual with a strong clinical background and expertise in clinical trial management, please review the following career opportunity.
Qualifications
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 4,000 people across almost 40 countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
Awards
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
EO/AA Employer M/F/Disability/Vets
#J-18808-Ljbffr
The latest news, articles, and resources, sent to your inbox weekly.
ResponsibilitiesWe are currently seeking aDirector, Feasibility, who will be an integral team leader within our global Proposals and Feasibility team. This position will evaluate and support new clinical trial opportunities by working strategically with Medpace Medical Experts, Clinical Trial Managers, and our Regulatory Submissions team. By collaborating with Investigators and...
Pharmiweb London
When our values align, there's no limit to what we can achieve. The Senior Director Epidemiology leads scientific contribution for epidemiology engagements and real-world studies, providing epidemiology content for proposals, capability presentations, bid-pursuit meetings, protocol development and analysis requirements. The Senior Director Epidemiology provides scientific guidance to Sponsors and internal...
Parexel Uxbridge
Business Development – DirectorUK based (Remote)Small Molecule Discovery, Development and CMC DivisionLead the Future of Drug DiscoveryDo you thrive on building strong relationships and driving profitable partnerships? Are you passionate about the life sciences industry and eager to contribute to groundbreaking advancements?Pharmaron, the leading Contract Research Organization (CRO), is seeking...
Pharmaron
Commercial Product ManagerCK Group are recruiting for a Commerical Product Manager on behalf of a medical diagnostic company to support the development of solutions that meet customer requirements across a broad range of applications. This role is 50% field based and 50% based in Gateshead. It is a permanent role...
CK Group Gateshead
Salary:£65,000 to £75,000 per annum (DOE) Contract Type:Full-Time, PermanentLocation:Cambridge, UK (flexible working options available)Closing date for applications:10th January 2025 for interviews from 20th January 2025Join Nu Quantum - Shaping the Future of TechnologyNu Quantum is at the forefront of quantum computing and advanced technology, driven by innovation, diversity, and a...
Nu Quantum Ltd Cambridge
Job overviewWe would like to recruit a Senior Trial Manager to cover a 12-month internal secondment in this very busy research office.Activity has been increasing following the stagnant period with pharmacy challenges and the DHR transformation programme. We now have several new complex studies early phase studies that are currently...
The Royal Marsden Sutton
