Clinical Research Coordinator - Onsite

pportunities that make their careers exciting, rewarding, and meaningful. With us, you're not just signing up for a contract you are joining a team that's got your back, answers your calls, and maybe even cracks a joke or two to brighten your day. Think of us as the travel buddy who handles the logistics while you focus on what you do best helping people heal.

Roles & Responsibilities
• Coordinate and manage multiple research protocols from feasibility through closeout
• Serve as the liaison between site personnel, sponsors, investigators, and the IRB
• Verify informed consent and protect study participant rights and safety
• Collect, review, and enter accurate source data into case report forms or EDC systems
• Track and report adverse events, deviations, and protocol waivers in a timely manner
• Create study-specific source documentation tools when needed and ensure data integrity
• Generate and track drug, device, and supply shipments to support study activities
• Attend monitoring visits, investigator meetings, and internal CRC meetings and respond to findings

Qualifications
• Certified Clinical Research Coordinator (CCRC) preferred or willingness to pursue certification
• Experience in clinical research coordination or an equivalent combination of education and experience
• Basic competency or training in ECG acquisition, phlebotomy, and specimen processing
• Familiarity with informed consent processes and human subjects protection
• Strong communication, organizational, and time management skills
• Attention to detail and the ability to follow study protocols precisely
• Comfort working on-site and collaborating with cross-functional teams

Education
• Associate's or Bachelor's degree in health sciences, nursing, biology, or related field preferred
• Or equivalent combination of education and clinical research experience

Knowledge & Skills
• Working knowledge of ICH guidelines and the Code of Federal Regulations (emerging understanding welcome)
• Familiarity with medical terminology and clinical trial procedures
• Data management skills and experience with electronic data capture or case report forms
• Ability to liaise effectively with sponsors, investigators, and institutional teams
• Competence in specimen handling, centrifuging, storing, and shipping procedures
• Strong interpersonal skills and self-motivation

Benefits
• Competitive pay and consistent weekly schedule to keep life balanced
• Supportive team environment that values professional growth
• Opportunities for certification support and training when required by protocol
• Flexible time off policies to recharge
• Travel reimbursement for occasional study-related travel
• Referral bonus program to reward great teammates
• Access to learning and development resources to grow your research skills
• A role where your attention to detail directly protects patient safety and data integrity

Travel Perks: Explore Asheville, NC

Explore Asheville's vibrant downtown with its arts district, farm-to-table restaurants, and craft breweries. Spend weekends at the Biltmore Estate, hike or scenic drive along the Blue Ridge Parkway, or take day trips to the Great Smoky Mountains for outdoor adventures. The area offers a lively cultural scene, local markets, and plenty of outdoor recreation to enjoy when you are off shift.

Apply Now

Ready to start your next adventure as a Research Coordinator? Let's get you moving forward!

Send your resume to [email protected] or call us at 408-441-9200 today.

Hashtags

#ResearchCoordinatorJobs #AshevilleNCJobs #ClinicalResearch #CRCJobs #UHCCareers #HealthcareJobs #ClinicalTrials #ContractJobs #AshevilleCareers #ResearchJobs