Contract Clinical Research Coordinator - PRN (Pharmacy Tech, RN, LPN Preferred)

Wake Research Corporation - Charleston, SC

Full-time - Entry Level

Charleston, SC

11-50 employees

Administrative and Support Services

About the position

The Clinical Research Coordinator (CRC) at M3 Wake Research is a contract position responsible for managing and facilitating daily clinical trial activities under the guidance of the Principal Investigator (PI). The CRC plays a critical role in ensuring that clinical trials are conducted in compliance with established protocols and regulatory standards, while also mentoring and overseeing other research staff. This role requires flexibility to support various study assignments as needed.

Responsibilities

• Assisting trial Investigator in screening and reviewing potential study participants' eligibility.
• Maintaining case report forms, charts, and documentation.
• Mentoring, training, and providing high-level oversight of other clinical research coordinators and research assistants.
• Ensuring that all clinical activities are carried out in accordance with established research protocols and compliance with applicable laws and regulations.
• Collecting and entering data as necessary.
• Assisting management with potential new hire selection and shadowing process.
• Assisting with study start-up, maintenance, and close-out of studies as needed.

Requirements

• 1-2 years of experience as a Clinical Research Coordinator.
• Phlebotomy experience is highly preferred.
• Previous experience as a medical assistant, LPN, or RN.
• Excellent verbal and written communication skills.
• Ability to learn quickly and understand complex protocols.
• Ability to follow detailed directions and multi-task effectively.
• Strict confidentiality maintenance of patients, employees, and company information in adherence to HIPAA guidelines.
• Extensive clinical trial knowledge through education and/or experience.
• Successful completion of GCP Certification and Advanced CRC preferred.
• Detail-oriented with familiarity with the Code of Federal Regulations regarding human subject protection.
• Strong interpersonal skills.