Site Relationship Coordinator
3 days ago
Job Summary
Our clinical activities are growing rapidly, and we are currently seeking a full-time Site Relationship Coordinator to join our vibrant Clinical Operations team. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network of sites, and develop key strategies to effectively conduct feasibilities in Singapore. This position will fit someone who has previous clinical research experience or perhaps a CRA who would like to reduce travel.
If you want an exciting career within a company that excels in delivering innovative research and development of cutting-edge drugs, where you can grow your potential, then this is the 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, site selection/alignment with studies 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;
Build and maintain 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;
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;
Broad knowledge of drug development, clinical trial management, and operational procedures, including GCP guidelines;
Demonstrated organizational and prioritization skills;
Demonstrated oral and written communication skills;
Proficient knowledge of Microsoft Office applications.
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 5,000 people across 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
Flexible work environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths with opportunities for professional growth
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Awards
Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
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
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