We are seeking Regulatory Compliance Coordinator to join us in the fight against cancer. In this role, you will work collaboratively as part of our research team focused on responsibilities related to managing clinical trials data. You will be a crucial member of our team as data is the key to our research, allowing us to continuously learn about the people and diseases we help treat.
* Collect, abstract, and enter data for research projects, databases, and/or protocols (clinical trials). This includes reviewing patient charts, existing databases, and other sources within a specified timeframe.
* Ensure data quality and integrity throughout the life of the study.
* Collaborate with research and care teams across MSK regarding data input.
* Generate data reports and deliver to all vital parties on the progress of the research project, database, or protocol.
* Design and/or enhance databases, data forms and tools. (e.g. patient/human subject calendars, schedules, tracking logs) to facilitate patient consent and specimen collection as needed for assigned research projects.
* Ensure all appropriate Institutional, State, and Federal regulations throughout the study are followed.
* Coordinate clinical research protocols and serve as the main point of contact, if applicable
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.