Clinical Research Coordinator managing the conduct of clinical trials at Emory University. Handling administrative activities and overseeing research project requirements and compliance.
About the role
- Clinical Research Coordinator at MSK, focusing on data collection and integrity for cancer research projects. Collaborating with multidisciplinary teams and ensuring compliance with regulations.
Responsibilities
- Collect, abstract, and enter data for research projects, databases, and/or protocols (clinical trials).
- 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 them to all vital parties on the progress of the research project, database, or protocol.
- Design and/or improve 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.
Requirements
- Healthcare/research experience is a plus.
- EPIC knowledge is a plus.
- Decision-making, with shown success at making timely decisions.
- Ability to hold yourself and others accountable to achieve goals and live up to commitments.
- Willing to take action and eager to embrace new opportunities and tough challenges.
- Resiliency in recovering from setbacks and skilled at finding detours around obstacles.
- Passion about medical terminology and science.
- Excellent communication skills.
- Enthusiasm and dedication to MSK's vision, mission, and values.
Benefits
- Health insurance
- Paid time off
- Flexible work arrangements
- Professional development opportunities
Job title
Job type
Experience level
Salary
Degree requirement
No Education Requirement
Location requirements
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