Iterative Health is looking to solve the problem of accelerating clinical research to transform patient outcomes in the field of gastrointestinal (GI) and hepatology novel therapies.
Requirements
- Knowledge of grammar, spelling, and punctuation.
- Knowledge of purchasing, budgeting, and inventory control.
- Skill in taking and transcribing dictation and operating office equipment.
- Skill in answering the phone and responding to questions.
- Ability to competently use Microsoft Office, including Word, PowerPoint, Excel, and appropriate practice management software.
Responsibilities
- Assists Study Team, as needed in communication of study requirements to all individuals involved in the study.
- Works with the Study Team, as needed to develop and implement recruitment strategies in accordance with TDDC RESEARCH and IRB requirements and approvals.
- Assists Study Team as needed in the screening of subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.
- Assists Study Team as requested to register participants in the Merge Clinical Trial Management System to ensure billing of study procedures to appropriate funding source.
- Maintains adequate inventory of study supplies. If handling investigational drugs/devices, follows the sponsor protocol and/or TDDC RESEARCH Policy on Investigational Drug/Device Accountability.
- Assists Study Team in completing study documentation and maintenance of study files in accordance with sponsor requirements and TDDC RESEARCH policies and procedures
- Review and update TDDC RESEARCH Study Workflow Chart and enter all patient visit data in e-CRF and Merge CTMS on a daily basis.
Other
- High school diploma or equivalent. Some college preferred.
- Minimum two years of experience with a health care organization.
- Must be able to lift up to 25 lbs.
- Must be able to travel and MVR
- Ability to work under pressure, communicate and present information.
