Clinical Research Coordinator – On-Site, Raleigh NC

M3 Wake Research; Raleigh (NC); On-site; USD 55,000 - 65,000; Full time

Benefits offered by this job

401(k), 401(k) matching

Dental insurance

Disability insurance

Employee assistance program

Flexible spending account

Health insurance

Life insurance

Paid time off

Vision insurance

Job summary

M3 Wake Research, an M3 company, is hiring a Clinical Research Coordinator for an on-site role in Raleigh, NC. The CRC collaborates with the Principal Investigator to manage day-to-day trial activities, ensuring protocol compliance and data integrity.

The CRC mentors staff, maintains regulatory documentation, screens participants, and helps with start-up and close-out activities. Strong knowledge of GCP and HIPAA, plus excellent communication, are essential.

Qualifications

• Clinical Research Coordinator with 1-2 years of experience
• Phlebotomy experience is highly preferred
• Excellent verbal & written communication skills
• Ability to learn quickly, read and understand complex protocols, follow very detailed directions, and multi-task
• Must be able to maintain strict confidentiality of patients, employees, and company information at all times and adhere to HIPAA Guidelines
• Extensive clinical trial knowledge through education and/or experience
• Successful completion of GCP Certification and Advanced CRC preferred
• Detail-oriented
• Familiarity with the Code of Federal Regulations as they pertain to human subject protection
• Strong interpersonal skills

Responsibilities

• Assist the Investigator in screening and reviewing potential study participant eligibility in accordance with protocol requirements
• Maintain accurate and timely case report forms, source documentation, study charts, and regulatory documentation
• Provide mentorship, training, and day-to-day oversight to Clinical Research Coordinators and Research Assistants
• Ensure all clinical research activities are conducted in compliance with study protocols, GCP guidelines, sponsor requirements, and applicable laws, regulations, policies, and procedures
• Collect, review, and enter study data with a high degree of accuracy and attention to detail
• Support management in the candidate interview, selection, onboarding, and shadowing processes for new hires
• Assist with study start-up activities, ongoing study maintenance, and close-out procedures across assigned studies and team initiatives
• Collaborate with investigators, sponsors, CROs, and internal departments to facilitate efficient study operations and issue resolution
• Demonstrate the ability to independently prioritize workload and adapt to changing study needs and assignments
• Serve as a resource for team members regarding study processes, protocol requirements, and site procedures

Skills

Clinical research knowledge

Communication skills

HIPAA compliance

Attention to detail

Multi-tasking

Confidentiality

Job description

M3 Wake Research, an M3 company, is hiring a Clinical Research Coordinator for an on-site role in Raleigh, NC. The CRC collaborates with the Principal Investigator to manage day-to-day trial activities, ensuring protocol compliance and data integrity.

The CRC mentors staff, maintains regulatory documentation, screens participants, and helps with start-up and close-out activities. Strong knowledge of GCP and HIPAA, plus excellent communication, are essential.