Clinical Research Coordinator - Clinical Research

Clinical Research Coordinator - Clinical Research CenExel is a leading clinical research organization specializing in Phase I to Phase IV trials across multiple therapeutic areas including Psychiatry, Acute Post‑Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Posted: Feb 16 Job Type: Full‑time Location: California Schedule: Monday – Friday (08:00 am – 4:30 pm) Hourly Range: $29.00 – $33.00 (depending on education, experience, and skillset) Job Summary: Responsible for coordinating clinical trials with strict adherence to ICH, GCP, protocol, and company guidelines, regulations, and policies. Essential Responsibilities and Duties Assist with coordinating all aspects of patient involvement from study initiation until 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 protocol development activities. Ensure site receives accurate information and supplies from sponsors (e.g., source, protocol, scales, supplies, approvals, contacts). Educate potential participants and caregivers on protocol specific details and expectations. Perform safety and efficacy assessments per protocol (vital signs, EKGs, blood draws, and other assessments as assigned). Assume other duties and responsibilities as assigned. Education, Experience, and Skills High school graduate or equivalent; Bachelor’s Degree preferred. 1+ years of experience as a Clinical Research Coordinator or similar position (Required). Phlebotomy experience (Highly Desired). Knowledge and understanding of federal regulations protecting human subjects in research and governing clinical trials. Strong leadership and mentorship skills. Developing and maintaining effective working relationships at all levels of the organization, sponsor, and vendor. Crisis management and problem‑solving skills; ability to react calmly and effectively in emergent situations. Works independently as well as part of a team. Effective verbal and written communication skills. Working Conditions Indoor office environment. Shift work, depending on location. Essential physical requirements include sitting, typing, standing, and walking. Lightly active position, occasional lifting up to 20 pounds; rarely over 20 pounds. Reporting to work, as scheduled, is essential. Overnight travel may be required for training and/or investigative meetings. CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status. #J-18808-Ljbffr SupportFinity™