Clinical Research Coordinator - Clinical Research

CenExel•Seal Beach, CA

10h•$62,000 - $75,000•Onsite

About The Position

The Clinical Research Coordinator assists with coordinating clinical trials while adhering to ICH, GCP, study protocols, company guidelines, regulations, and policies. The role supports patient involvement from study initiation through completion, organizes research information, observes subjects, assists with data analysis and reporting, schedules data collection, and maintains research quality and compliance. It also includes documenting adverse events and protocol deviations, performing administrative and regulatory duties, participating in protocol development activities, and ensuring the site receives accurate information and supplies from sponsors. The coordinator educates potential participants and caregivers about protocol expectations and performs protocol-required safety and efficacy assessments, such as vital signs, EKGs, and blood draws. The position is scheduled Monday through Friday, 8:00 a.m. to 4:30 p.m. The work is primarily in an indoor office environment. Shift work may depend on location, and overnight travel may be required for training or investigative meetings. The salary range is $62,000–$75,000 annually, depending on education, experience, and skillset.

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 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 data collection.
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 studies as appropriate.
Participate in other protocol development activities.
Ensure the site receives accurate information and supplies from sponsors, including source documents, 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.