Clinical Research Coordinator II, RN

About Care Access Care Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow. With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all. To learn more about Care Access, visit www.CareAccess.com. How This Role Makes a Difference The CRC II, RN conducts delegated clinical tasks and monitoring of research participants in accordance with Good Clinical Practices (GCP), ensuring protocol and regulatory compliance. How You'll Make An Impact Patient Coordination Prescreen study candidates Obtain informed consent per Care Access Research SOP . Complete visit procedures in accordance with protocol. Complete basic clinical procedures, such as blood draws, vital signs, ECGs, etc. Review laboratory results, ECGs, and other test results (e.g., MRIs) for completeness and alert values, ensuring investigator review in a timely fashion. Discuss study medication, required procedures, eligibility criteria and impact on office flow with Investigator and site staff. Prioritize activities with specific regard to protocol timelines Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials. Coordinate and attend pre-study site visits, site initiation visits, and monitor visits with clinical staff and Sponsor/CRO representatives. Identify adverse events (AEs) and Serious Adverse Events (SAEs) and promptly notify Principal Investigator and Sponsor (where appropriate) Balances protocol needs with patient experience; proactively addresses concerns. Mentors CRC I peers; provides onboarding and day‑to‑day guidance. Moderate complexity; mixed visit types, active IP and AE/SAE workflows. Can operate as solo CRC onsite. Conducts delegated clinical tasks (RN specific) and monitoring of research participants in accordance with Good Clinical Practices (GCP), ensuring protocol and regulatory compliance. Clinical Tasks Preparation and administration of Investigational Product (IP; study drug) Monitor participant for adverse reactions Perform phlebotomy and insert IV catheters Conduct delegated clinical procedures as required per protocol Maintain Investigational Product records in accordance with regulations and sponsor requirements. Maintain the blinding of all study products where required. Maintain proper storage, security and temperature for all medications and investigational products. Documentation Record data legibly and enter in real time on paper or e-source documents Accurately record study medication inventory, medication dispensation, and patient compliance. Resolve data management queries and correct source data within sponsor provided timelines Assist regulatory personnel with completion and filing of regulatory documents. Assist in the creation and review of source documents. Patient Recruitment Assist with planning and creation of appropriate recruitment materials. Assist in development of recruitment plan and obtain listing of potential candidates to contact from subject database. Actively work with recruitment team in calling and recruiting subjects Review and assess protocol (including amendments) for clarity, logistical feasibility Ensure that all training and study requirements are met prior to trial conduct. Communicate clearly verbally and in writing. Attend Investigator meetings as required. Ensure adequate supplies have arrived on site for protocol initiation (lab kits, study medication, specialized equipment, IVRS/EDC access and passwords) Interact in a positive, professional manner with patients, sponsor representatives, investigators and Care Access Research personnel and management. Maintain effective relationships with study participants and other care Access Research personnel. Owns studies; prioritizes competing demands; mentors CRC I. The Expertise Required Ability to understand and follow institutional SOPs. Working knowledge of medical and research terminology Working knowledge of federal regulations, good clinical practices (GCP) Excellent phlebotomy skills Ability to communicate and work effectively with a diverse team of professionals. Team Collaboration Skills: Work effectively and collaboratively with other team members to accomplish mutual goals. Bring positive and supportive attitude to achieving these goals. Ability to work independently in a fast-paced environment with minimal supervision. Strong organizational skills: Able to prioritize, delegate, direct, support, assign and evaluate others work and follow through on assignments. Communication Skills: Strong verbal and written communication skills as evidenced by positive interactions with coworkers, management, clients, and vendors. Operates independently for most study activities; escalates complex issues as needed. Manages stakeholder communications; facilitates visits and meetings. Team Collaboration Skills: Work effectively and collaboratively with other team members to accomplish mutual goals. Bring positive and supportive attitude to achieving these goals. Strong computer skills Ability to balance tasks with competing priorities. Critical thinker and problem solver. Curiosity and passion to learn, innovate, able to take thoughtful risks and get things done. Friendly, outgoing personality; maintain a positive attitude under pressure. High level of self-motivation and energy. Ability to work independently in a fast-paced environment with minimal supervision. Must have a client service mentality. Certifications/Licenses, Education, and Experience Minimum Education: A minimum of 3 years prior Clinical Research Coordinator experience required Minimum Experience: Prefer 1 year of experience as a Care Access Research Clinical Research Coordinator Recent phlebotomy experience required Minimum 1 year of experience as a RN required Licenses: RN license in good standing required. Phlebotomy and infusion experience required. How We Work Together Location: This role is onsite. Travel: This role requires up to 80% regional (within 100 miles) travel requirements further explained below. Length of travel will depend upon study requirements, staff needs, and company initiatives. Physical demands associated with this position Include: The ability to use keyboards and other computer equipment. Walking - 20% Standing - 20% Sitting - 20% Lifting - 20% Up to 25lbs Over 25lbs Overhead Driving - 20% The expected pay range for this role is $75,000 - $110,000 USD per year for full time team members. Benefits & Perks (US Full Time Employees) Paid Time Off (PTO) and Company Paid Holidays 100% Employer paid medical, dental, and vision insurance plan options Health Savings Account and Flexible Spending Accounts Bi-weekly HSA employer contribution Company paid Short-Term Disability and Long-Term Disability 401(k) Retirement Plan, with Company Match Mandatory Employer Disclosures Notice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction. Notice

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