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 and deep expertise in clinical trials combined with cutting-edge AI.
Requirements
- Ability to competently use Microsoft Office, including Word, PowerPoint, Excel, and appropriate practice software.
- CRC certification preferred.
- Minimum 4 or more years of clinical research experience.
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.
- 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.
- Protects the rights and welfare of all human research participants involved in research in accordance with Federal regulations
Other
- 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.
- High school diploma/GED certificate required.
