Clinical Research Coordinator I

CBH Health, LLC, CenExel CBH, 9318 Gaither Rd., Suite 220, Gaithersburg, MD 20877, USA. About the Company CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. It specializes in CNS and early phase studies, offering 18 science‑led Centers of Excellence. Recently acquired by BayPine Capital Partners, CenExel provides medical and scientific support in the design and execution of clinical trials, along with patient engagement, data analytics, and integrated operations. Job Summary Responsible for assisting with coordinating clinical trials in strict adherence to ICH, GCP, protocol, and company guidelines, regulations, and policies. Compensation 26.90–34.35 per hour 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 protocol development activities. Ensure site receives accurate information and supplies from sponsors (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 as 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. Developing and maintaining 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. 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 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. Equal Employment Opportunity 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 status, or disability. This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor. #J-18808-Ljbffr