Clinical Research Site Relationship Coordinator
medpaceDayton, OH
Clinical Research Site Relationship Coordinator
medpaceDayton, OH
49 days ago
Industries
Research and Development in the Physical, Engineering, and Life SciencesResearch and Development in BiotechnologyOther Scientific and Technical Consulting ServicesAbout the role
Job Summary:
The Site Relationship Coordinator is a new role within the Clinical Monitoring team at Medpace that offers the opportunity to have an exciting career in the research of drug and medical device development. This position works to develop collaborative relationships with investigators and site personnel to establish new and ongoing site relationships, as well as support the Strategic Proposal Development staff with feasibility assessments in accordance with feasibility processes and deliverable timelines. For those with a clinical research background who are looking to make a difference, this could be the right opportunity for you.
Responsibilities:
Serve as site relations and excellence partner by providing oversight and building/retaining relationships of assigned sites within assigned country; Support Management in conducting/expediting feasibility activities (standalone, blinded, initial, ongoing), site selection/alignment with studies and/or therapeutic areas, and study start-up; Proactively research and understand specified site landscape/intelligence (KOL presence and knowledge, site capabilities, country standard of care and medical practices, etc.) as it relates to specific patient population, recruitment, and retention; Building and maintaining relationships with preferred site networks/flagship sites which includes facilitating master CDAs and holding meetings with network directors as needed; Provide ongoing support of sites, including identifying and discussing future new business; Develop effective plans for site contacts, troubleshooting, and follow-up; Serve as main point of contact for project teams regarding site performance issues and updates on pertinent site information; and May be responsible for other projects and responsibilities as assigned, including site Qualification Visits, prepping/consultation support for site audits, etc.
Qualifications:
Bachelor's degree and 1-2 years of Clinical Monitoring experience; Ability to travel
Matching similar jobs
JOB OVERVIEW
Experience level
Senior
Location
Dayton, OH
Occupation
Clinical Research Coordinators
Industry
Research and Development in the Physical, Engineering, and Life Sciences
Posted
49 days ago
Tired of running searches?
Rank the roles you'd take once, and matches like these arrive on their own.
CREATE PROFILE (opens in a new tab)