Clinical Research Coordinator: Impactful Trials & Compliance

CenExel; Los Alamitos (CA); On-site; USD 62,000 - 75,000; Full time

Benefits offered by this job

Health Insurance

Dental

Vision

LTD

STD

Life Insurance

401k

Job summary

CenExel Clinical Research in California seeks a Clinical Research Coordinator to support coordination of complex clinical trials across phases. You will work with investigators, sponsors, and vendors to ensure protocol adherence and data integrity in an on-site environment.

The ideal candidate has 1+ years of CRC experience, solid knowledge of ICH/GCP, regulatory requirements, and strong communication skills.

Qualifications

• 1+ years of experience as a Clinical Research Coordinator.
• Knowledge of Federal regulations protecting human subjects.
• Ability to work independently and as part of a team.
• Strong communication skills.

Responsibilities

• Coordinate all aspects of patient involvement from study initiation to completion.
• Organize research information for clinical trials.
• Observe subjects and assist with data analysis and reporting.
• Schedule data collection and ensure data integrity.
• Document adverse events and protocol deviations.
• Ensure site compliance with sponsorships, protocols, and approvals.
• Educate participants on protocol details and expectations.
• Perform safety and efficacy assessments per protocol.

Skills

CR Coordinator experience

ICH/GCP knowledge

Regulatory understanding

Communication skills

Education

Bachelor's degree

Job description

CenExel Clinical Research in California seeks a Clinical Research Coordinator to support coordination of complex clinical trials across phases. You will work with investigators, sponsors, and vendors to ensure protocol adherence and data integrity in an on-site environment.

The ideal candidate has 1+ years of CRC experience, solid knowledge of ICH/GCP, regulatory requirements, and strong communication skills.