Preparation of targeted reviews/profile of outliers, search and summarize information relevant for various clinical documents preparation. Serve as a resource to address medical questions or clarify issues arising during conduct of the study.
In this role, the selected candidate will contribute routine scientific knowledge or expertise to research and development activities for achievement of project goals and solve routine experimental design or research problems with some assistance.
In this role, the selected candidate must have a hands-on experience using molecular biology techniques including PCR and real-time PCR to evaluate clinical samples in a hospital, CRO, reference laboratory, or similar environment.
In this role, you will ensure appropriate clinical safety assessment and risk management of compounds. Conduct real-time oversight of ongoing trials to identify and mitigate patient, study design, data or study conduct issues.
In this role, the selected candidate must have an experience in a hospital, research lab, reference lab, or similar environment working as a Medical Technologist or similar; experience with lab techniques such as: PCR (polymerase chain reaction), qPCR, Gel Electrophoresis, etc.