Clinical Research Coordinator: Lead Trials & Compliance

M3Usa; Los Angeles (CA); On-site; USD 70,000 - 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 USA is seeking a Clinical Research Coordinator in Los Angeles to support daily trial activities under the guidance of the Principal Investigator. You will screen participants, maintain case report forms, and help with study start-up and close-out.

Ideal candidates have 2+ years of CRC experience, strong communication, and familiarity with HIPAA and CFR. GCP certification and phlebotomy credentials are a plus. This role offers comprehensive benefits and a competitive salary.

Qualifications

• 2+ years of Clinical Research Coordinator experience.
• Certification in phlebotomy strongly preferred.
• Excellent verbal & written communication skills.
• Ability to learn quickly, read complex protocols, and multi-task.
• Maintain strict confidentiality and adhere to HIPAA.
• Extensive clinical trial knowledge and CFR familiarity.
• GCP certification and Advanced CRC preferred.
• Detail-oriented with strong interpersonal skills.

Responsibilities

• Assist trial investigators in screening potential participants for eligibility.
• Maintain case report forms, charts and study documentation.
• Mentor and oversee other coordinators and assistants.
• Ensure activities follow protocol, laws, policies and regulations.
• Collect and enter data as needed.
• Support study start-up, maintenance and close-out activities.

Skills

Communication

Attention to detail

HIPAA knowledge

Interpersonal skills

Clinical trial knowledge

GCP knowledge

Multi-tasking

Education

GCP Certification

Phlebotomy certification (preferred)

Job description

M3 USA is seeking a Clinical Research Coordinator in Los Angeles to support daily trial activities under the guidance of the Principal Investigator. You will screen participants, maintain case report forms, and help with study start-up and close-out.

Ideal candidates have 2+ years of CRC experience, strong communication, and familiarity with HIPAA and CFR. GCP certification and phlebotomy credentials are a plus. This role offers comprehensive benefits and a competitive salary.