Iterative Health is looking to hire a Clinical Research Coordinator (CRC) to support the acceleration of clinical research in gastrointestinal (GI) and hepatology novel therapies by empowering research teams and study sponsors with tech-enabled services.
Requirements
- Minimum 2-3 years of Clinical Research coordinating experience required.
- Ability to competently use Microsoft Office, including Word, PowerPoint, Excel, and appropriate practice management software.
Responsibilities
- Implements recruitment strategies to prescreen, screen, and enroll subjects in active trials.
- Screen subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.
- Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis.
- Complete study documentation and maintenance of study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.
- Manage the day to day activities of the study including problem solving, communication and protocol management.
- Ensure all safety data is reviewed by the PI in a timely manner.
- Protect the rights and welfare of all human research participants involved in research.
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.
- Bachelor’s Degree preferred
