GI Alliance is seeking an experienced Clinical Research Coordinator II.
Duties of this position include, but are not limited to, the following:
Position purpose
The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the Site Manager and Principal Investigator (PI). The CRC supports, facilitates, and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.
Responsibilities/Duties/Functions/Tasks:
- Regular communication of study requirements and changes to relevant members of study staff. 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 participants eligibility or exclusion.
- Acts as a point of reference for study participants by answering questions and keeping them informed of study progress.
- Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis. Maintains adequate inventory of study equipment and supplies onsite at all times.
- 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.
- Maintains ongoing communication with sponsor, research participants, Site Manager and PI throughout the course of the study.
- 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.
- Protects the rights and welfare of all human research participants involved in research.
- Other duties as assigned.