Clinical Trials Coordinator: Phase I–IV Research

CenExel Clinical Research; Los Angeles (CA); On-site; USD 39,000 - 43,000; Full time

Job summary

CenExel Clinical Research in Sherman Oaks, CA is seeking a Full-Time Clinical Research Coordinator to support trial activities in line with ICH, GCP, protocol, and sponsor guidelines.

The role coordinates patient involvement, data collection, safety assessments, and regulatory duties across the study lifecycle, with a Monday–Friday schedule. On-site work with potential travel, compensation $28.00–$31.00 per hour depending on education and experience.

Qualifications

• 1+ years of experience as a Clinical Research Coordinator (Required)
• Bachelor's Degree preferred
• Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials
• Strong leadership and mentorship skills
• Ability to communicate verbally and in writing
• Works independently as well as part of a team

Responsibilities

• Assist with coordinating all aspects of patient involvement from study initiation until study completion
• Organise research information for clinical trials
• Observe subjects and assist with data analysis and reporting
• Schedule the collection of data
• Document adverse events, protocol deviations, and other unanticipated problems appropriately
• Report research data to maintain quality and compliance
• Perform administrative and regulatory duties related to the study as appropriate
• Participate in other protocol development activities
• Ensure site receives accurate information and supplies from sponsors

Skills

Clinical Research Coordinator exposure

Leadership skills

Mentorship skills

Verbal & written communication

Crisis management

Teamwork

Education

Bachelor's Degree

Job description

CenExel Clinical Research in Sherman Oaks, CA is seeking a Full-Time Clinical Research Coordinator to support trial activities in line with ICH, GCP, protocol, and sponsor guidelines.

The role coordinates patient involvement, data collection, safety assessments, and regulatory duties across the study lifecycle, with a Monday–Friday schedule. On-site work with potential travel, compensation $28.00–$31.00 per hour depending on education and experience.