CRA to Site Relationship Coordinator jobs in United States
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Medpace ยท 2 days ago

CRA to Site Relationship Coordinator

Medpace is a full-service clinical contract research organization (CRO) that provides Phase I-IV clinical development services. The Site Relationship Coordinator will develop collaborative relationships with investigators and site personnel to support feasibility assessments and ensure ongoing site relationships.

BiotechnologyPharmaceutical

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

Qualification

Clinical Monitoring experienceDrug development knowledgeClinical trial managementGCP guidelines knowledgeMicrosoft Office proficiencyOrganizational skillsProblem-solving skillsCommunication skills

Required

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
Demonstrated 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
Proficient knowledge of Microsoft Office applications

Benefits

Flexible work environment
Competitive PTO packages, starting at 20+ days
Competitive compensation and benefits package
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Community involvement with local nonprofit organizations
Discounts on local sports games, fitness gyms and attractions
Modern, ecofriendly campus with an on-site fitness center
Structured career paths with opportunities for professional growth
Discounted tuition for UC online programs

Company

Medpace, Inc., a clinical research organization, provides clinical development services for pharmaceutical and biotechnology

Funding

Current Stage
Public Company
Total Funding
unknown
2016-08-10IPO
2014-02-24Acquired

Leadership Team

J
Jesse Geige
President
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Company data provided by crunchbase