Registered Nurse (RN) - Clinical Research

Clinical Research Coordinator

Full-time, 5x8 days, Days (08:00 - 17:00), Hybrid option available.

Assignment Details

Temporary to permanent position, candidate should ideally have a local commute of 30 minutes or less.

Requirements

• Minimum of five years of experience in a clinical research setting managing patients.
• Experience in patient-facing clinical trials is required.
• Blood Draw Certification is required (must be a phlebotomist, MA, LVN, or RN).
• Must possess Epic experience and strong computer skills (including Outlook, MS Teams, Word, and Excel).
• Certification as CCRC (ACRP) preferred.
• Neurological conditions experience is a plus.
• Spanish or Korean speaking skills are a plus.

Responsibilities

• Support investigators during the conduct of multiple clinical research trials.
• Coordinate enrollment, study visits, and follow-up care of patients participating in clinical trials.
• Act as the liaison between sponsors, regulatory agencies, patients, investigators, nurses, and staff during trials.
• Assist in training new research assistants and Clinical Research Coordinators as needed.
• Conduct all transactions in compliance with applicable regulations, policies, and procedures.
• Maintain professional appearance and conduct at all times.
• Maintain organizational and patient confidentiality at all times.

Benefits

• Medical, Dental, Vision Insurance After 90 Days
• Accrued PTO
• Continuing Education through TLC Academy & Relias Training
• Referral Bonus up to $1,000
• 401(k) with Match
• Access to Purchase Aflac
• Employee Assistance Program (EAP)
• Discounts on Travel and Retail through Employee Discount Network
• Life Insurance
• TLC ShiftShield income protection for eligible travelers between assignments

Compliance / Notes

Parking details will be provided.