Start Date: 01-12-2025

Contract Type: Travel Contract

Candidate Pay Rate: $35 per hour

About United Health Care Staffing

At United Health Care Staffing (UHC Staffing), we believe healthcare staffing should be more than just finding a job. We are here to connect amazing professionals with opportunities 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 multiple research protocols from initiation through close-out, keeping timelines on track
• Serve as the primary liaison with local investigators and study sponsors to facilitate smooth communication
• Assist with regulatory documentation and submission activities to support compliance
• Maintain accurate study records and track participant-related documentation with attention to detail
• Support research operations by helping implement study procedures and resolving logistical challenges
• Collaborate with cross-functional teams to monitor study progress and escalate issues as needed
• Contribute to process improvements and best practices for human subjects research

Qualifications

• Experience or coursework in coordinating research protocols, clinical research, or related internships preferred
• Familiarity with human subjects protections and regulatory compliance (IRB processes, informed consent basics)
• Completion of research-related training such as CITI or GCP is a plus
• Strong written and verbal communication skills for sponsor and investigator interactions
• Organizational skills with the ability to manage multiple tasks and priorities
• Comfort working under supervision while building independent responsibility

Knowledge & Skills

• Research protocol coordination and study administration
• Human subjects research principles and protections
• Regulatory compliance and documentation practices
• Sponsor communication and investigator liaison duties
• Basic research operations and study logistics
• Strong attention to detail and effective communication

Benefits

• Supportive team environment that helps you grow your research career
• Opportunities to build experience with protocol coordination and sponsor communication
• Access to professional development and training (think GCP/CITI refreshers)
• Flexible onboarding and mentorship under direct supervision
• Paid time off and work-life balance resources (details discussed during interview)
• Licensure/certification assistance and reimbursement where applicable
• Employee assistance and wellness programs to keep you at your best
• A collaborative culture that values your contributions and development

Hashtags

#ResearchCoordinatorJobs #ClinicalResearch #NonClinicalRoles #UHCCareers #ResearchJobs #RegulatoryCompliance #HumanSubjectsResearch #ContractJobs #ClinicalTrials #ResearchOperations