Clinical Research Coordinator I

About Us CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science‑led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world‑class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process. We offer an exceptional work environment that promotes teamwork, positive leadership, and optimal work‑life balance, and provide highly competitive compensation of $26‑27/h, with a generous benefits package for full‑time employees after 30 days of employment including Health, Dental, Vision, LTD, STD, Life Ins, and 401k. Job Summary Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH, GCP, protocol, and company guidelines, regulations, and policies. Compensation $26.90‑$34.35 /hr depending on education, experience and skillset Essential Responsibilities And Duties Assist with coordinating all aspects of patient involvement from study initiation until 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 site receives accurate information and supplies from sponsors (e.g., source, protocol, scales, supplies, approvals, contacts, etc.). 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. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered all-inclusive. Education / Experience / Skills High school graduate or equivalent; Bachelor’s Degree preferred. 0‑3 years of experience in the medical field. Knowledge and understanding of federal regulations protecting human subjects in research and that govern the conduct of clinical trials. Strong leadership and mentorship skills. Develop and maintain effective working relationships at all levels of the organization, along with those at the sponsor and vendor level. Crisis management and problem‑solving skills; ability to react calmly and effectively in emergent situations. Works independently as well as functioning as part of a team. Must be able to effectively communicate verbally and in writing. Working Conditions Indoor, office environment. Shift work, depending on location. Essential physical requirements include sitting, typing, standing, and walking. Lightly active position, occasional lifting of up to 20 pounds. Rarely lift 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 CenExel