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.
Responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required.
The Clinical Research Coordinator is responsible for managing and assisting the Principal Investigator(s) and research team in the coordination of all activities of the study as required for successful implementation of the study protocol(s).
In this role, you will be responsible to perform site monitoring visits in accordance with the study monitoring plan to ensure compliance with the investigational plan, monitoring plan, applicable regulator.
The main responsibilities include consenting patients prior to surgery, providing the tissue bank proper notification and documentation of consent, and managing regulatory components of the neuro logic tissue banking protocols and clinical data collection and management currently open at these hospitals.
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.
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.