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 will prepare and review project and study documents including clinical trial protocols, clinical study reports, patient SAE narratives, clinical sections of registration dossier documents (ISS, ISE, Investigator Brochure, etc.).
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 perform a wide variety of moderately and highly complex tasks and analysis of human fluids and tissues, using manual procedures as well as operating various laboratory equipment and automated analyzer systems.
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.