Clinical Research Coordinator - Clinical Research

CenExel•Bellflower, CA

7h•$30 - $34•Onsite

About The Position

The Clinical Research Coordinator assists with coordinating clinical trials while adhering to ICH, Good Clinical Practices, study protocols, and company guidelines, regulations, and policies. The role supports patient involvement throughout the study, organizes trial information, observes participants, assists with data analysis and reporting, and helps maintain research quality and compliance. The coordinator also performs administrative and regulatory study duties, supports protocol development activities, ensures the site receives accurate sponsor information and supplies, educates potential participants and caregivers about study requirements, and conducts protocol-based safety and efficacy assessments. The position is based in an indoor office environment and requires scheduled attendance. Overnight travel may be required for training or investigative meetings.

Requirements

High school graduate or equivalent.
At least 1 year of experience as a Clinical Research Coordinator.
Knowledge and understanding of federal regulations protecting human subjects in research and governing the conduct of clinical trials.
Strong leadership and mentorship skills.
Ability to develop and maintain effective working relationships at all levels of the organization and with sponsors and vendors.
Crisis management and problem-solving skills, including the ability to react calmly and effectively in emergent situations.
Ability to work independently and as part of a team.
Effective verbal and written communication skills.

Nice To Haves

Bachelor's degree.

Responsibilities

Assist with coordinating all aspects of patient involvement from study initiation through study completion.
Organize 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 the site receives accurate information and supplies from sponsors, including source materials, protocols, scales, supplies, approvals, and contacts.
Educate potential participants and caregivers on protocol-specific details and expectations.
Perform safety and efficacy assessments per protocol, including vital signs, EKGs, blood draws, and other assigned assessments.
Assume other duties and responsibilities as assigned.