Location: Staten Island,NY, USA
Job DetailsJob LocationLOC022 RBA Richmond Behavioral Associates - Staten Island, NYSalary Range$30.00 - $34.00 Sr. CRC-FTTitle: Senior Clinical Research Coordinator Location: Staten Island, NYAbout us:ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with expertise in early and late-stage neuroscience drug development. With 20 wholly owned clinical sites and 4 affiliated sites, we conduct in-patient and out-patient phase I-IV clinical research studies. ERG has 400+ in-patient beds, a large and growing database of patients suffering from mental illness, neurological disorders, sleep disorders, addictions, Acute and Chronic Pain, diabetes, and other illnesses as well as normal healthy volunteers who participate in trials for the advancement of medicine. With access to over 32 million patients/subjects and 5000 + completed trials, ERG continues to grow its capabilities and expand into indications where there are tremendous unmet medical needs in the United States and globally.RBA conducts trials covering the full range of CNS diagnoses including Depression, Anxiety, Bipolar Disorder, Schizophrenia, Alzheimer's Disease and Insomnia.Job Description:The Senior Clinical Research Coordinator will complete all study related procedures and distribute study medication and instructions to research subjects under the direction of the Principal Investigator and the Site Director. They will maintain accurate, confidential files and documentation of study participants. In executing these position responsibilities, the Clinical Research Coordinator is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.Responsibilities:Gain thorough knowledge of study protocols with the Principal Investigator and Site Director before study start.Act as lead coordinator, supervising staff, and collaborating with CRAs and company personnel.Assist Site Director with marketing as needed.Draft and review source documents for accuracy before study initiation.Develop recruitment strategies and maintain communication with staff.Manage all trial aspects, including compliance and enrollment programs.Train and mentor support staff, contribute to SOPs, and address protocol issues.Study Management:Perform tasks under Principal Investigator supervision.Attend investigator meetings and manage IRB renewals.Ensure protocol adherence, document breaches, and regulatory communication.Screen, enroll, and schedule subjects; obtain consent.Maintain accurate study records and report adverse events.Complete study close-out procedures.Skills and Qualifications:High School Diploma (College degree preferred), 7+ years as Clinical Research Coordinator.Familiarity with GCP, ICH guidelines, and medical terminology.Certified coordinator with strong communication and computer skills (Word, Excel, proprietary apps).#MedHP