Clinical Research Site Relationship Coordinator
medpaceDayton (OH)
Clinical Research Site Relationship Coordinator
Posted 54 days ago
medpaceDayton (OH)
Clinical Research CoordinatorsResearch and Development in the Physical, Engineering, and Life Sciences
SENIORITY
Senior
About 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
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