Clinical Research Coordinator
Current- Works closely with the Vice President for Research in various studies — ie. clinical trials, review, observational studies, and meta-analysis.- Participates in funding activities such as proposal writing, submission of proposals, and determining funding sources- Generate study-related documentation, protocols, and reports.- Submits required documents to the institutional review board and assists in the overseeing operations to ensure compliance to protocols- Supports in assessing patients for inclusion and exclusion criteria to evaluate eligibility and comprehension- Assist in the informed consent discussion and document refusals in accordance with protocol.- Tracks adverse event and side effect data and collaborate with the multidisciplinary team to coordinate patient care.- Liaison with study stakeholders such as study sponsor, university departments, satellite facilities, and respondents- Assist with the processing and summarization of data using Microsoft excel and statistical software.