Clinical Trials Coordinator II - Patient-Centric Research

NATIONAL CLINICAL TRIALS INC; Los Angeles (CA); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

401(k)

Paid time off

Job summary

National Clinical Trials Inc. in Los Angeles, CA seeks a motivated Clinical Research Coordinator II to coordinate and manage active clinical trials, ensuring protocol adherence and data integrity.

You will interact with sponsors, CROs, and IRBs while maintaining strict compliance with FDA regulations and GCP/ICH guidelines. The role requires a Bachelor's degree in life sciences or related field and 2+ years of CRC experience, with proficiency in EDC systems (REDCap, Medidata Rave) and CTMS.

Qualifications

• Bachelor's degree in life sciences, healthcare, or a related field is required.
• Minimum 2+ years of experience as a Clinical Research Coordinator (CRC).
• Solid knowledge of GCP, ICH guidelines, FDA regulations, and HIPAA compliance.
• Experience with EDC systems (REDCap, Medidata Rave) and CTMS platforms.
• ACRP (CCRC) or SOCRA (CCRP) certification preferred.
• Strong organizational skills with exceptional attention to detail and accuracy.
• Excellent interpersonal and communication skills for working with patients and research teams.
• Ability to manage multiple protocols simultaneously in a fast-paced research environment.

Responsibilities

• Coordinate and manage day-to-day operations of clinical trials in compliance with FDA regulations, GCP, and ICH guidelines.
• Screen, enroll, and follow up with study participants while ensuring protocol adherence.
• Collect, record, and maintain accurate study data in EDC systems and source documents.
• Serve as a primary point of contact for sponsors, CROs, and IRB communications.
• Prepare and submit regulatory documents, including IRB submissions, amendments, and continuing reviews.
• Monitor patient safety and report adverse events (AEs) and serious adverse events (SAEs) per protocol requirements.
• Collaborate with principal investigators, sub-investigators, and multidisciplinary clinical teams.
• Support site initiation visits, monitoring visits, and audits conducted by sponsors or regulatory agencies.

Skills

Attention to detail

Communication

Multitasking

Team collaboration

Education

Bachelor's degree in life sciences or related field

Tools

REDCap

Medidata Rave

CTMS

Job description

National Clinical Trials Inc. in Los Angeles, CA seeks a motivated Clinical Research Coordinator II to coordinate and manage active clinical trials, ensuring protocol adherence and data integrity.

You will interact with sponsors, CROs, and IRBs while maintaining strict compliance with FDA regulations and GCP/ICH guidelines. The role requires a Bachelor's degree in life sciences or related field and 2+ years of CRC experience, with proficiency in EDC systems (REDCap, Medidata Rave) and CTMS.