Onsite Clinical Research Coordinator - Mentorship & Growth

M3 USA Corporation; Wilmington (NC); Vor Ort; USD 45.000 - 65.000; Vollzeit

Benefits dieser Stelle

401(k) matching

Dental insurance

Disability insurance

Employee assistance program

Flexible spending account

Health insurance

Life insurance

Paid time off

Vision insurance

Zusammenfassung

M3 Wake Research in Wilmington, NC is seeking a Clinical Research Coordinator to support daily trial activities under the supervision of the site management and PI. The CRC will manage screening, data collection, and documentation while ensuring adherence to protocol, HIPAA, and regulatory requirements.

Ideal candidates have 1–2 years of clinical research experience, familiarity with GCP, and strong communication skills to mentor staff and coordinate with investigators and sponsors.

Qualifikationen

• 1-2 years of clinical research experience.
• Phlebotomy experience preferred.
• Experience as medical assistant, LPN, or RN helpful.
• Excellent verbal and written communication skills.
• Ability to learn quickly, read complex protocols, and multi-task.
• Maintain strict confidentiality and HIPAA compliance.
• Known with GCP and regulatory standards.

Aufgaben

• Screen and review potential study participants for eligibility.
• Maintain case report forms, charts and documentation.
• Mentor and oversee other coordinators and research assistants.
• Ensure activities comply with protocol, laws, and guidelines.
• Collect and enter data as needed.
• Assist management with new hire selection and shadowing.
• Support study start-up, maintenance, and close-out activities.
• Be flexible with study assignments.

Kenntnisse

Clinical Research

GCP Certification

Phlebotomy

HIPAA Knowledge

Communication

Confidentiality

Jobbeschreibung

M3 Wake Research in Wilmington, NC is seeking a Clinical Research Coordinator to support daily trial activities under the supervision of the site management and PI. The CRC will manage screening, data collection, and documentation while ensuring adherence to protocol, HIPAA, and regulatory requirements.

Ideal candidates have 1–2 years of clinical research experience, familiarity with GCP, and strong communication skills to mentor staff and coordinate with investigators and sponsors.