Clinical Research Coordinator - Clinical Research

CenExel•Los Angeles, CA

1d•$28 - $31•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 from study initiation through completion, organizes trial information, observes subjects, assists with data analysis and reporting, and schedules data collection. It also includes documenting adverse events and protocol deviations, reporting research data to support quality and compliance, and performing study-related administrative and regulatory duties and other protocol development activities. The coordinator ensures the site receives accurate information and supplies from sponsors, educates potential participants and caregivers about protocol details and expectations, and performs protocol-based safety and efficacy assessments such as vital signs, EKGs, and blood draws. Other duties may be assigned. The position is based in an indoor office environment. Work includes sitting, typing, standing, and walking, with occasional lifting of up to 20 pounds and rare lifting over 20 pounds. Shift work may depend on location; the listed schedule is Monday through Friday, 8:00 a.m. to 4:30 p.m. Overnight travel may be required for training or investigative meetings, and attendance as scheduled is essential.

Requirements

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 organizational levels 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.
High school graduation or equivalent.

Nice To Haves

Bachelor's degree preferred.

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 materials, protocols, scales, supplies, approvals, and contacts.
Educate potential participants and caregivers about 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.