Clinical Research Coordinator - Clinical Research

CenExel•Sherman Oaks, CA

9h•Onsite

About The Position

The Clinical Research Coordinator assists with coordinating clinical trials in accordance with ICH, GCP, study protocols, and company guidelines, regulations, and policies. The role supports participants throughout the study, organizes research information, schedules data collection, and helps maintain the quality and compliance of clinical trial data. It also includes documenting adverse events and protocol deviations, performing administrative and regulatory tasks, and supporting protocol development activities. The coordinator helps ensure the site receives accurate study information and supplies from sponsors, educates potential participants and caregivers about protocol-specific details, and performs assigned safety and efficacy assessments, which may include vital signs, EKGs, and blood draws. The position is based in an indoor office environment and may require shift work depending on location and overnight travel for training or investigative meetings. The stated schedule is Monday through Friday, 8:00 a.m. to 4:30 p.m. The hourly pay range is $28.00–$31.00, 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 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.

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 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.