TI Clinical Research Assistant II
Posted Updated
Description
- Coordinates with OPAM and Contracts office during budget and contract negotiation process
- Coordinates with DoM office and OPAM for account maintenance, invoicing, and reconciliation.
- Actively screens and consents patients for the studies and conduct study visits. This will include coordinating appointments with the PI and/or sub-PI as needed.
- Submit modification approvals to the IRB and complete all other IRB reportorial requirements
- Completes electronic data entry for research patients in a timely manner
- Maintains and organize study binders, as well as prepare for site visits and meet with monitors.
- Participates in recruitment activities for active studies.
- Coordinates care of research patients with their specialists/PCPs
- Bachelor's in relevant field OR
- Associate's AND
2 years of relevant experience OR
3 years of relevant experience OR
Equivalent combination of training and experience - Must have excellent communication, organization, and customer service skills, and must be a self-starter.
- Proficient knowledge of Microsoft Office Suite (including Word, Outlook, and Excel); strong organizational skills; excellent oral and written communication skills; meticulous detail to data and study procedures; ability to prioritize work demands and trouble shoot; ability to work independently in a multi-task environment. Familiarity with health record database systems is helpful.
- Bachelor’s degree with major courses in the field of research is preferred.
- Prior research experience in a university setting.
- Prior clinical research experience in a complex health system or university setting
Basic clinical examination & vital signs assessment is preferred.
Phlebotomy training is preferred.
Familiarity with health record and research database systems.