Sr Clinical Research Coordinator at Joulé

Title: Clinical Research Coordinator Location: Manchester, NH Type/Duration: Contract, 6 month/renewable, 100% onsite Schedule: Monday-Friday, core daytime business hours based on clinic hours, could have some earlier morning starts Start Date: ASAP Joule is currently looking to hire a Clinical Research Coordinator to work onsite in Manchester, NH. You must have at least 1 year of experience working as a CRC within drug trials. Summary of Key Responsibilities Primary responsibility is to screen, enroll, and follow study subjects ensuring protocol compliance and monitoring while the subjects are on study. Responsible for all data collection, source documentation, completing study-specific case report forms, and submission of adverse experience reports. Duties and Responsibilities Duties include but are not limited to: Supports enrolling patients onto the clinical trial through screening, enrollment and follow up of eligible subjects according to protocol requirements Ensures the protection of study patients by verifying informed consent procedures and adheres to protocol requirements/compliance Collects, completes, and enters data into study-specific case report forms or electronic data capture systems Ensures timely and accurate data completion Collects blood samples and tracks shipments and requests supplies as needed Implements study-specific communications Ensures timely adherence to protocol requirements Responsible for completion of all required documentation Maintains accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, subject logs and study-related communications Communicates all study-related issues to appropriate study colleagues or manager Apprises principal investigator and management of all study-specific medical issues for guidance Attends study-specific meetings as required or asked to do so Reviews and responds to any monitoring findings and escalates issues Requirements Bachelor's degree required, Master’s degree preferred CCRC preferred 1+ years of relevant clinical trials experience, 5+ years preferred Must have clinical research/trials experience (CRC experience needed) Fundamental understanding of medical and research operations terminology (nice to have) Recognize circumstances requiring prompt escalation to PI, IRB, or Supervisor (nice to have) Ref: #568-Clinical