Clinical Research Coordinator

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

The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the guidance of the clinical research site management and Principal Investigator (PI). While the PI is primarily responsible for the overall conduct of the clinical trial, the CRC manages, supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.

Essential Duties and Responsibilities:

• Assisting trial Investigator in screening and review of potential study participants eligibility
• Maintaining case report forms, charts and documentation
• Mentoring, training, and high-level oversight of other clinical research coordinators and research assistants
• Ensuring that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirements
• Collecting and entering data as necessary
• Assist management with potential new hire selection and shadowing process
• Assist with study start-up, maintenance, and close-out of studies as needed for those on the team
• Ability to be flexible with study assignments

Clinical Research Coordinator with 2+ years of experience

• Certified in phlebotomy is strongly preferred
• Excellent verbal & written communication skills
• Ability to learn quickly, read and understand complex protocols, follow very detailed directions, and multi-tasking
• 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

About M3:

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Benefits:

• 401(k), 401(k) matching
• Dental insurance
• Disability insurance
• Employee assistance program
• Flexible spending account
• Health insurance
• Life insurance
• Paid time off
• Vision insurance
• *This position offers a competitive pay rate of $70,000-$90,000/yr.
• *M3 reserves the right to change this job description to meet the business needs of the organization