Senior Research Coordinator - Non-Clinical

UHC Staffing

Brentwood, TNFull-time

34 an hour

Behavioral Health Market Context

Apply Nowvia UHC Staffing

Benefits

Paid Time OffDental CoverageHealth Insurance

Job Description

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 multiple research protocols from enrollment through close-out, keeping studies on track and compliant
• Serve as the primary liaison with local investigators, Sponsors, and study teams to ensure clear communication
• Support regulatory document preparation and submission to maintain compliance with institutional and sponsor requirements
• Assist with participant screening, informed consent processes, and scheduling study visits
• Collect, document, and manage study data accurately to support high-quality research outcomes
• Monitor protocol adherence and support quality assurance activities and audits
• Contribute to a culture of continuous learning by maturing your understanding of research operations and regulations

Qualifications
• Bachelor’s degree in a life science, public health, nursing, or related field preferred (or equivalent experience)
• Experience coordinating clinical or non-clinical research protocols preferred
• Familiarity with human subjects research principles and regulatory requirements (IRB, informed consent)
• Comfortable acting as a sponsor and investigator liaison with strong written and verbal communication skills
• Detail-oriented, organized, and capable of managing multiple tasks and timelines
• Willingness to work onsite and collaborate closely with local investigators and study teams

Education
• Bachelor’s degree in a life science, public health, nursing, or related field preferred
• CITI or GCP training recommended (or willingness to obtain)

Knowledge & Skills
• Research coordination and protocol management
• Regulatory compliance and human subjects research knowledge
• Strong stakeholder communication with investigators and Sponsors
• Research operations and documentation best practices
• Ability to learn and apply institutional and sponsor procedures quickly

Benefits
• Generous housing and travel support to help you settle in comfortably
• Comprehensive medical, dental & vision coverage to keep you well
• Paid time off so you can recharge and come back energized
• Licensure assistance and reimbursement for required training
• Supportive team environment that values professional growth
• Professional development and opportunities to advance your research career
• Travel reimbursement and logistics support for contract assignments
• A friendly onboarding process and a mentor to help you hit the ground running

Travel Perks: Explore Brentwood, TN

Brentwood is a leafy, welcoming suburb with easy access to Radnor Lake State Park and the hiking trails at Percy and Edwin Warner Parks—perfect for weekend nature escapes. Enjoy nearby Franklin’s historic downtown with boutique shops, live music venues, and great dining. Nashville’s legendary music scene, museums, and cuisine are a short drive away for quick city adventures between shifts.

Apply Now

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

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

Hashtags

#SeniorResearchCoordinatorJobs #BrentwoodTNJobs #ResearchJobs #ClinicalResearch #UHCCareers #ContractTravel #NonClinicalResearch #ResearchCoordinator #HealthcareJobs #NashvilleAreaJobs

Qualifications

  • Familiarity with human subjects research principles and regulatory requirements (IRB, informed consent)
  • Comfortable acting as a sponsor and investigator liaison with strong written and verbal communication skills
  • Detail-oriented, organized, and capable of managing multiple tasks and timelines
  • Willingness to work onsite and collaborate closely with local investigators and study teams
  • CITI or GCP training recommended (or willingness to obtain)
  • Research coordination and protocol management
  • Regulatory compliance and human subjects research knowledge
  • Strong stakeholder communication with investigators and Sponsors
  • Research operations and documentation best practices
  • Ability to learn and apply institutional and sponsor procedures quickly

Benefits

  • Candidate Pay Rate: $34 per hour
  • Generous housing and travel support to help you settle in comfortably
  • Comprehensive medical, dental & vision coverage to keep you well
  • Paid time off so you can recharge and come back energized
  • Licensure assistance and reimbursement for required training
  • Supportive team environment that values professional growth
  • Professional development and opportunities to advance your research career
  • Travel reimbursement and logistics support for contract assignments
  • A friendly onboarding process and a mentor to help you hit the ground running

Responsibilities

  • Coordinate multiple research protocols from enrollment through close-out, keeping studies on track and compliant
  • Serve as the primary liaison with local investigators, Sponsors, and study teams to ensure clear communication
  • Support regulatory document preparation and submission to maintain compliance with institutional and sponsor requirements
  • Assist with participant screening, informed consent processes, and scheduling study visits
  • Collect, document, and manage study data accurately to support high-quality research outcomes
  • Monitor protocol adherence and support quality assurance activities and audits
  • Contribute to a culture of continuous learning by maturing your understanding of research operations and regulations


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