Onsite Clinical Research Coordinator II — Raleigh

M3 USA Corporation; Raleigh (NC); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

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 is actively seeking a Clinical Research Coordinator II for our Wake Research site in Raleigh, NC. You will collaborate with the PI and site management to oversee day-to-day trial activities, ensuring protocol compliance, data integrity, and efficient workflow across studies.

The role requires at least 2 years of CRC experience, strong communication, and a solid understanding of GCP/CFR. On-site duties involve mentoring staff, regulatory upkeep, and coordinating start-up through

Qualifications

• 2+ years of clinical research coordination experience.
• Phlebotomy experience is highly preferred.
• Excellent verbal and written communication skills.
• Strong knowledge of GCP and CFR requirements.

Responsibilities

• Assist Investigator in screening participant eligibility per protocol.
• Maintain accurate case report forms, source docs, and regulatory files.
• Mentor and supervise CRCs and research assistants.
• Ensure study activities comply with protocols, GCP, sponsor rules, and laws.
• Collect and review study data with high accuracy.
• Support candidate interviews, onboarding, and shadowing.
• Assist with study start-up, maintenance, and close-out tasks.
• Collaborate with investigators, sponsors, CROs, and internal teams.
• Prioritize workload and adapt to changing study needs.
• Serve as a resource on study processes and site procedures.

Skills

CRC experience

Communication skills

HIPAA knowledge

Job description

M3 Wake Research is actively seeking a Clinical Research Coordinator II for our Wake Research site in Raleigh, NC. You will collaborate with the PI and site management to oversee day-to-day trial activities, ensuring protocol compliance, data integrity, and efficient workflow across studies.

The role requires at least 2 years of CRC experience, strong communication, and a solid understanding of GCP/CFR. On-site duties involve mentoring staff, regulatory upkeep, and coordinating start-up through