Site Relationship Coordinator

				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 5,000 people across 40+ countries.

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 
* Broad knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines;
* Demonstrated organizational and prioritization skills;
* Demostrated ability to problem-solve and practice independent decision-making;
* Demonstrated oral and written communication skills, as well as ability to maintain relationships with both external and internal teams; and 
* Proficient knowledge of Microsoft Office applications.
			

Apply

Share this job:

Share this Job

View company profile

Medpace, Inc.

Connect To Our Company