Clinical Research Coordinator RN

CAN Community Health • Las Vegas, NV

3d • $73,000 - $82,000

About The Position

CAN Community Health is now hiring a Clinical Research Coordinator RN Schedule: Full-Time | Day Shift | Monday-Thursday 8:00 am - 5:00 pm Friday 8:00 am - 12:00 pm Are you passionate about patient care and ready to make a difference every day? We are looking for someone who is passionate about serving the needs of individuals impacted by HIV, Hepatitis C, STI's, and other infectious diseases. You will become part of our professional team that drives home our Company's Mission and Values. We have received recognition for more than six (6) years NPT's Best Non-Profit to Work for Award. Why You’ll Love It Here Competitive pay Generous paid PTO and Sick time 11 Paid Company Holidays Paid training and certification support Health, dental, vision, with generous company contribution, paid life and disability plans & retirement plan with generous match of up to 8% of your contribution additional match of 1%. Tuition Reimbursement Plan Other voluntary plans are available to support you and your family Career growth opportunities in a supportive environment Salary : Starting $73,000 - 82,000 annually based on education and experience. What You’ll Do The Clinical Research Coordinator RN (CRCRN) independently manages the planning, execution, and oversight of complex clinical trials in compliance with federal regulations, institutional policies, and sponsor requirements. This role serves as a subject matter expert and strategic partner to Principal Investigators, playing a key role in study design feasibility, regulatory submissions, operational workflows, and oversight of participant safety and data integrity. The CRC exercises independent judgment and discretion in the coordination and execution of multiple research studies across multiple sites, ensuring all research activities support scientific, ethical, and compliance standards. Coordinates with the PI, and the Director of Clinical Research (DCR); collaborating agencies, administration, and departments to help ensure that the clinical research and related activities are performed in accordance with Federal regulations and sponsoring agency policies and procedures. Collaborates with the PI and DCR to develop materials and tools necessary to appropriately train study participants in the conduct of the study around issues of protocol requirements, schedule of visits, and compliance. Ensures training is completed and documented according to all requirements Serves as the primary liaison between sponsors, IRB, and internal stakeholders to ensure study goals are achieved and issues are proactively resolved. Responsible for investigational product (IP) handling, including preparation, reconstitution, and administration in accordance with protocol specifications; perform IV catheter placement and initiate infusion of IP under appropriate clinical supervision and guidelines. Oversees day-to-day execution of study protocols, ensuring alignment with study objectives and regulatory requirements. Evaluates protocol feasibility, complexity, and resource needs in collaboration with the PI and DCR. Assists PI and DCR in the communication of study requirements and training compliance to all team members involved in conducting the study. Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion. Ensures adherence to protocol-defined safety assessments and monitors for adverse events, exercising clinical judgment in escalation and documentation. Assesses, records and reports symptoms, reactions, treatments, and changes in clinical trial participant conditions. Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of an employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

Requirements

• Bachelor’s degree in nursing (RN) preferred, Minimum is associate's degree in nursing (RN)
• Minimum 3–5 years of progressively responsible experience in clinical trial coordination, preferably across multiple therapeutic areas
• CPR Certified
• Must be able to operate a motor vehicle and have valid insurance and driver’s license.
• Must be able to pass a Level I and Level II Background check as required.

Responsibilities

• The Clinical Research Coordinator RN (CRCRN) independently manages the planning, execution, and oversight of complex clinical trials in compliance with federal regulations, institutional policies, and sponsor requirements.
• Serves as a subject matter expert and strategic partner to Principal Investigators, playing a key role in study design feasibility, regulatory submissions, operational workflows, and oversight of participant safety and data integrity.
• Exercises independent judgment and discretion in the coordination and execution of multiple research studies across multiple sites, ensuring all research activities support scientific, ethical, and compliance standards.
• Coordinates with the PI, and the Director of Clinical Research (DCR); collaborating agencies, administration, and departments to help ensure that the clinical research and related activities are performed in accordance with Federal regulations and sponsoring agency policies and procedures.
• Collaborates with the PI and DCR to develop materials and tools necessary to appropriately train study participants in the conduct of the study around issues of protocol requirements, schedule of visits, and compliance.
• Ensures training is completed and documented according to all requirements
• Serves as the primary liaison between sponsors, IRB, and internal stakeholders to ensure study goals are achieved and issues are proactively resolved.
• Responsible for investigational product (IP) handling, including preparation, reconstitution, and administration in accordance with protocol specifications; perform IV catheter placement and initiate infusion of IP under appropriate clinical supervision and guidelines.
• Oversees day-to-day execution of study protocols, ensuring alignment with study objectives and regulatory requirements.
• Evaluates protocol feasibility, complexity, and resource needs in collaboration with the PI and DCR.
• Assists PI and DCR in the communication of study requirements and training compliance to all team members involved in conducting the study.
• Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.
• Ensures adherence to protocol-defined safety assessments and monitors for adverse events, exercising clinical judgment in escalation and documentation.
• Assesses, records and reports symptoms, reactions, treatments, and changes in clinical trial participant conditions.

Benefits

• Competitive pay
• Generous paid PTO and Sick time
• 11 Paid Company Holidays
• Paid training and certification support
• Health, dental, vision, with generous company contribution, paid life and disability plans & retirement plan with generous match of up to 8% of your contribution additional match of 1%.
• Tuition Reimbursement Plan
• Other voluntary plans are available to support you and your family
• Career growth opportunities in a supportive environment

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree
• Number of Employees: 251-500 employees