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Full-time
bachelor degree
Competitive compensation programs, Health benefits, Wellness benefits, Retirement benefits, Paid time off, On-site fitness and wellness facilities
Posted 10d ago
Apply by Sep 1
~40 hrs/week
Responsibilities
The Site Relationship Coordinator manages and retains relationships with clinical research sites while supporting feasibility assessments and study start-up activities. They serve as the primary point of contact for project teams regarding site performance and intelligence.
Requirements
Candidates must hold a bachelor's degree and possess 1-2 years of clinical monitoring experience. Proficiency in drug development procedures, GCP guidelines, and Microsoft Office is required, along with the ability to travel up to 20% of the time.
Full job description
Clinical Research Coordinators wanted at Medpace! Become a Site Relationship Coordinator and join our growing team!
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 <20% to research sites nationwide is required;
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.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
Leadership throughout Medpace is both accessible and approachable
Continuous Growth & Development
Office based environment with on-site mentors
Defined career paths with clear advancement opportunities
Industry renowned onboarding and training programs designed to accelerate professional development
Ongoing training and continuous learning opportunities throughout your career
An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
Competitive compensation programs that recognize and reward performance
Comprehensive health, wellness, retirement, and PTO benefits
Office based culture with occasional WFH that provides flexibility for eligible positions after training
Company-sponsored social events and intramural sports
Cincinnati Headquarters Experience
A modern corporate campus designed to support collaboration and productivity
Multiple on-site dining options in the heart of Madison Square
Free on-site parking
Convenient access to on-site 24-7 fitness and wellness facilities
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
Accelerating Drug, Biologic and Medical Device Clinical Development
Industry
Pharmaceutical Manufacturing
Company size
5,001-10,000 employees
Founded
1992
Headquarters
Cincinnati, OH
LinkedIn followers
377,549
Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 6,500 people across 46 countries.
Offices: 5375 Medpace Way, Cincinnati, OH 45227, US
Early Phase Clinical ResearchPhase II-III Clinical ResearchRWE-Late Phase Clinical ResearchMedical Device and DiagnosticsRegulatory AffairsMedical WritingClinical MonitoringClinical Trial ManagementBiostatistics and Data SciencesDrug Safety and Pharmacovigilance
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