Senior Clinical Research Coordinator-Sr. CRC

3 weeks ago

Dayton, United States Evolution Research Group Full time

Job DetailsJob LocationLOC017 MCRC Midwest Clinical Research Center - Dayton, OHSr. CRC-FTTitle: Senior Clinical Research Coordinator Location: Dayton, OHAbout 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.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:Obtain detailed knowledge of all components of each study protocol through review and analysis of study information with Principal Investigator and Site Director prior to the effective date of the study.Actas head coordinator responsible for supervising and coordinating others working on protocols and interfacing with CRA and company personnel assigned to that study.Develop draft source documents and review the documents for accuracy and clarity prior to study start up.Develop a mechanism for subject recruitment and ongoing communications with PCP and nursing staff as appropriate.Sound conduct of the clinical trial, including but not limited to recruitment, screening, enrollment, and follow up of eligible subjects according to protocol requirements.Review with Principal Investigator and Site Director, any components of the study for which additional information or clarification are required prior to the initiation of the study.Organizational management of all aspects of the trial, including but not limited to caseload and study files.Manage studies with sponsor, and Principal Investigator to ensure compliance with protocol requirements.Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment. Study Management Perform study activities as delegated by the Principal Investigator and under the supervision of the Site Director.Attend the investigator meeting for each assigned protocol, as appropriate.Completion of IRB study renewals and maintain copies of all IRB communications.In conjunction with Site Director and Principal Investigator, ensure adherence to the protocols and document breaches or violations with sponsors and appropriate Institutional Review Boards (IRBs) and other outside regulatory organizations, as required.Screen, enroll subjects and schedule subject visits in conjunction with Principal InvestigatorReview and obtain informed consent from with potential study volunteers.Document all written and phone correspondences with sponsor, labs, IRB other regulatory organizations.Maintain organized, accurate and complete study records including but not limited to regulatory documents, signed informed consents, IRB correspondence/approvals, source documentation, drug dispensing logs, subject logs and study-related communications.Assist Principal Investigator in conducting studies in manner to ensure integrity of data and safety of subjects.Enter data as appropriate for protocol (paper-electronic data capture)Ensure timely and accurate CRF completion for each study subject.In conjunction with Principal Investigator, accurately report and track adverse events as defined by each study protocol.Outcomes of enrollment and sponsor monitoring visits of all assigned protocolsPerform study close-out procedures.Store study records appropriatelyAdditionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG's objectives.Skills and Qualifications:Education and experienceHigh School Diploma or its equivalent; College degree preferred.5+ years of experience as a Clinical Research Coordinator Understands regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference on Harmonization (ICH) guidelines.Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner. Knowledgeable in medical terminology to communicate with physician office and laboratory staff. Demonstrate the initiative to act independently, initiating activity as required and making appropriate decisions within the constraints of study protocols, regulatory requirements, and company policy.Able to initiate or modify behavior to achieve desired outcomes despite environmental factors, priorities, or problems that might not be well defined or that are subject to change.RequirementsUnderstand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines. Knowledgeable in medical terminology Excellent communication skills (interpersonal, written, verbal) Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)#HP

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