Iterative Health is looking to accelerate the path to market for gastrointestinal (GI) and hepatology novel therapies by empowering their partner sites with tech-enabled services, combining deep expertise in clinical trials with cutting-edge AI.
Requirements
- Minimum 1-2 years of clinical research experience.
- Ability to competently use Microsoft Office, including Word, PowerPoint, Excel, and appropriate practice management software.
Responsibilities
- Screen subjects for eligibility using protocol specific inclusion and exclusion criteria.
- Entry of participant information and study visit procedures into the Clinical Trial Management System to ensure billing to appropriate funding source.
- Maintains adequate inventory of study supplies.
- When handling investigational drugs/devices, follows the sponsor protocol and/or Impact Research Policy on Investigational Drug/Device Accountability.
- Complete study documentation and maintenance of study files in accordance with sponsor requirements and Impact Research policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms.
- Collects and reports ongoing patient recruitment/ enrollment metrics to Director and PI.
- Arranges secure storage of study documents that will be maintained according to Good Clinical Practice guidelines or for the contracted length of time, whichever is longer.
Other
- High school diploma/GED certificate required.
- Perform quality work within deadlines with or without direct supervision.
- Interact professionally with other employees, customers and suppliers.
- Work effectively as a team contributor on all assignments.
- Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations.
