The Clinical Research Coordinator work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. The CRC will be responsible for the primary data collection and management of patient clinical information as …
Read more about ""The Regulatory Coordinators (RC) works under the direction of the Principal Investigator(s), Clinical Research Manager and / or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project. The RC coordinates aspects of protocol submissions, prepares and submits regulatory documents, and maintains records on …
Read more about ""The Research Project Manager II (RPM) is responsible for assigned day-to-day coordination and overall management of sponsor activities for assigned clinical trials Sponsor activities include coordinating trial startup and site startup activities, safety event tracking and reporting, deviation/violation tracking and reporting, participant accrual tracking and reporting, and/or conducting teleconferences. The …
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