The CRC1 coordinates, completes and monitors the daily clinical trial activities and performs a variety of duties involved in the collection, compilation, documentation and reporting of clinical research data.
In this role, you will collaborate with nursing staff and Principal Investigator ( PI ) ascertains pretreatment and eligibility requirements; interviews participants and obtains social and medical histories; based on results determines and registers participants with appropriate sponsors; completes informed consent; determines and organizes patient's treatment and test schedules.
The Research Coordinator is an entry-level role for candidates with research experience and who have a bachelors degree in behavioral or quantitative social sciences or a related subject. You will work as part of a team responsible for delivering insights and ad effectiveness measurement.
In this role, you will be responsible for lab/study budget & inventory including purchasing of supplies & services ensuring that they are necessary, reasonable & project related; orders & maintains inventory of study supplies & may distribute intra-departmental charges.
In this role, the selected candidate will be responsible for recruitment and screening of study subjects, obtaining informed consent, enrollment of subject in research study, subject follow-up, collecting and analyzing research data, completion of the case report form (CRF), adverse event reports and ensuring protocol adherence.