Clinical Research Coordinator (On-site)

M3USA•Wilmington, NC

7d•Onsite

About The Position

The Clinical Research Coordinator (CRC) is a specialized research professional who works under the guidance of clinical research site management and the Principal Investigator (PI). While the PI is primarily responsible for the overall conduct of a clinical trial, the CRC manages, supports, facilitates, and coordinates daily trial activities and plays a critical role in study conduct. This on-site position is located in Wilmington, North Carolina.

Requirements

1–2 years of experience as a Clinical Research Coordinator.
Previous experience as a medical assistant, LPN, or RN.
Excellent verbal and written communication skills.
Ability to learn quickly, read and understand complex protocols, follow detailed directions, and multitask.
Ability to maintain strict confidentiality of patient, employee, and company information and adhere to HIPAA guidelines.
Extensive clinical trial knowledge through education and/or experience.
Detail-oriented.
Familiarity with the Code of Federal Regulations as it pertains to human subject protection.
Strong interpersonal skills.

Nice To Haves

Phlebotomy experience is highly preferred.
Successful completion of GCP Certification and Advanced CRC preferred.

Responsibilities

Assist the trial Investigator with screening and reviewing potential study participants for eligibility.
Maintain case report forms, charts, and documentation.
Mentor, train, and provide high-level oversight to other clinical research coordinators and research assistants.
Ensure clinical activities follow established research protocols and comply with applicable laws, regulations, policies, and procedures.
Collect and enter data as necessary.
Assist management with potential new-hire selection and shadowing.
Assist with study start-up, maintenance, and close-out as needed for team studies.
Remain flexible with study assignments.