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, 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.
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.
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.
Developing sample prep methodology from various matrices (e.g. biological fluids, blood spots, etc.) compatible with LC-MS including protein precipitation, liquid-liquid extraction, solid phase extraction and affinity enrichment.
coordinating the flow of patients as well as managing the human and material resources of the Department, during specified shift, in order to provide quality patient care and an environment conducive to staff growth and satisfaction