Iterative Health is looking to accelerate the path to market for gastrointestinal (GI) and hepatology novel therapies by empowering research sites with tech-enabled services and AI-driven solutions to improve patient outcomes.
Requirements
- Ability to competently use Microsoft Office, including Word, PowerPoint, Excel, and appropriate practice management software.
Responsibilities
- 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.
- Manages the day to day activities of the study including problem solving, communication and protocol management.
- 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.
- Minimum 1-2 years of clinical research experience.
- Must be able to lift up to 25 lbs.
- Must be able to travel and MVR
- Occasional evening and weekend work.
