CRC/CRN

Location: Norfolk, VA

Role Summary

Seeking a dedicated Clinical Research RN or Coordinator to manage and execute clinical trial operations for oncology and cellular therapy studies. This role involves direct interaction with study participants, close collaboration with principal investigators, and comprehensive protocol compliance management. Approximately 80% of the daily responsibilities are computer- and data-based, with direct patient care remaining limited in non-RN coordinator capacities.

Key Responsibilities

• Patient Screening & Enrollment: Present study concepts, objectives, and treatment details to potential clinical trial participants; perform detailed screening and eligibility assessments. Participate in the informed consent process and formally enroll eligible patients on protocol.

• Protocol & Care Coordination: Coordinate patient care plans to adhere strictly to study protocol requirements. Oversee physician order preparation to ensure full protocol compliance.

• Physician & Investigator Collaboration: Partner with physicians to evaluate patient changes in condition, record concomitant medications, manage dose modifications, track responses to study treatments, and report adverse events.

• Regulatory Compliance & Monitoring: Collect and maintain essential regulatory documentation in compliance with standard operating procedures and applicable federal regulations. Schedule, host, and interact with monitors and auditors during site visits.

• Sponsor & Partner Communication: Maintain direct communication and workflow alignment with research sponsors, study bases, and external research partners.

Qualifications & Requirements

• Education: Graduate from an accredited nursing education program (BSN preferred).

• Licensure & Certifications: Current RN licensure in Virginia preferred. Active BCLS or ACLS certification required. OCN, SoCRA, or ACRP certifications preferred.

• Experience: Minimum of one (1) year of nursing experience, preferably within oncology. Prior experience in clinical research operations, investigational drug studies, or cellular therapy trials preferred.

• Technical Skills: Strong experience with electronic data capture (EDC) systems, computer data entry, and research database management.

• Core Competencies: Ability to analyze and interpret technical procedures, protocols, and regulatory documents; excellent written and oral communication skills.

For California Applicants:

We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO) , and the California Fair Chance Act (CFCA).

This position is subject to a background check based on its job duties, which may include patient care, working with vulnerable populations, access to financial and confidential information, driving, working with heavy machinery, or working in a warehouse or laboratory environment. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.

Here at Medix, we are dedicated to providing workforce solutions to clients throughout multiple industries. We have been named among the Best and Brightest Companies to Work For in the Nation for two consecutive years. Medix has also been ranked as one of the fastest growing companies by Inc. Magazine.

Our commitment to our core purpose of positively impacting 20,000 lives affects not only the way we interact with our clients and talent, but also with our co-workers! The goal is lofty, but it is made attainable through the hard work and dedication of our teams and their willingness to lock arms together. Are you ready to lock arms with us?