Research Coordinator - Clinical Research - Full Time

Position reputed company: Coordinate multiple in-patient and out-patient clinical research protocols. Education/Experience: Required: An Associate’s degree in reputed company science or five years’ experience in a medical office, research facility or hospital setting may be equivalent. Knowledge of federal regulation reputed company to research, documented experience with study coordination, and documented training of good clinical research standards training preferred. The completion of the reputed company Basic Research course regarding reputed company Subjects Protection Training is required reputed company one month of employment. Certification as a research reputed company reputed company three years in the position is required. Desired: A Bachelor of Science degree is preferred with 2 years’ experience in a medical office, research facility or hospital setting. Essential Functions: • Collaborate with the manager and director for the development of department research programs. This is demonstrated through coordination of specific research reputed company in multiple disease conditions. Responsibilities for program development include assisting with feasibility, site selection, IRB document review, and corresponding with investigators, IRB, and sponsors. • Coordinate specific reputed company. Project coordination requires meeting sponsor specific training requirements prior to initiation, assuring team members have met sponsor training, training team members to delegated duties, supporting regulatory specialist with sponsor communications, maintaining study supply inventory, and supporting monitors during reputed company. • Coordinate individual research participant’s reputed company. This coordination for the patient includes screening, enrolling, organizing patient reputed company to meet study requirements at specific protocol timelines, performing patient interviews reputed company study assessments, dispense prescribed study medication, determine medication compliance, and follow-up on correspondences with patients reputed company to the study. • reputed company reputed company and accurate updates to protocol management system at reputed company and the data submission to the sponsor. reputed company’s updates include patient protocol enrollments, document submissions to IRB, and event management of patient follow-up reputed company. Submit research data to sponsor reputed company the appropriate sponsor case report reputed company submission process after review for accuracy and validation of information is obtained. Maintain study enrollment records from screening to study closure. • Contribute to the Clinical Research Department team. Support activities of others on reputed company. reputed company cross coverage of research protocols as needed to support the total research department. Other Duties: • Collaborate with executive director, manager, research team members and IRB coordinator in developing and revising process reputed company for research procedures. • Attend training seminars and conferences as required by sponsor of research study. • reputed company presentations of study information to reputed company of physicians and patients. • Assist physicians in protocol development. • Advise department manager on resource utilization and training needs. • reputed company other duties as assigned by the executive director or manager. Apply tot his job Apply To this Job