The Research Project Manager (RPM) is responsible for assigned day-to-day coordination and overall management of activities for assigned clinical trials. Activities include coordinating trial startup and site startup activities, providing training to participating site research staff, regulatory submissions, safety event tracking and reporting, deviation/violation tracking and reporting, participant accrual tracking …
This position's work location is fully remote with the ocassional time onsite as needed. The Sr. Medicare Coverage Analyst (MCA) is responsible for reviewing clinical research protocols, Informed Consent Forms, Clinical Trial Agreements, and other relevant study-related documents to create a coverage analysis/billing guide. The coverage analysis indicates which …
The Clinical Research Coordinator work within the Center of Cancer Therapeutic Innovation (CCTI) 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 …
Read more about ""The Regulatory Coordinators (RC) works under the direction of the Principal Investigator(s), Regulatory Operations Manager and / or directly for the Clinical Trials Office to complete the regulatory requirements of the GYN Oncology clinical research project. The RC coordinates aspects of protocol submissions, prepares and submits regulatory documents, and maintains …
Read more about ""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 …
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