Job Description
Overview
Responsible for pre-clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment, specimen collection and transmittal, data collection and management, adverse event management to ensure protocol compliance in conjunction with the PI, clinical team and clinical research nurses and team.
Responsibilities - Assist in new IRB application and annual renewal process of COG, local and other multi-institutional protocols.
- Enter data on Hematology, Oncology and Stem Cell Transplant patients on computerized data capture forms.
- Manage communications - mail, phone, fax, e-mail for COG, local and multi- institutional studies.
- Act as liaison between NYMC and Westchester Medical Center, regarding new study requirements.
- Assist in creating and illustrating quality improvement and compliance measures.
- Collect and report vital Bone Marrow Transplant data to internal and external agencies.
- Maintain and update important master lists and distribute them to the division on a regular basis.
- Maintain follow-up on projects/reports and inform, the department head of critical situations.
- Develop data capture forms.
Qualifications Education requirement: Master's preferred.
Maximum Salary USD $20,384.00/Yr.
Minimum Salary USD $16,307.00/Yr.
Job Tags
Full time, Local area,