Assistant Study Operations

About the role

The Assistant, Study Operations will provide administrative support and will work with the Study team to execute clinical trial activities. Responsibilities of the Assistant, Study Operations include preparation of clinical trial related documents and execution of tasks/clinical activities in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs). What You'll Do Here Ensure the confidentiality of clinical trial participants and sponsors is respected. Maintain and advocate a high level of customer service and quality within the department. Assist in the maintenance of clinical trial source. Preparation, filing, assisting with updates and archival of trial related source. Assist with preparation, handling, distribution, tracking and maintenance of clinical trial related supplies. Perform protocol specific activities, including but not limited to vital signs and electrocardiograms. Obtain and document study related events and data in compliance with GCP/SOPs. Proactively communicate issues and/or problem resolutions to departmental supervisors and managers. Complete and maintain training as required per job needs. What You'll Need to Succeed High School diploma or GED required; college degree and related job experience preferred. Microsoft Suite experience required. EMR/EHR system experience preferred. Great customer service experience. Excellent written and verbal communication Able to work in a fast-paced environment