Alexandra Manea Email and Phone Number

I am responsible for running the clinical trial according to the study protocol. Together with the investigator, work ensures the safety of the participants and the integrity of the data collected.I perform a range of different tasks, such as:•Managing ethics submissions;•Creating study specific data collection forms;•Scheduling participant study visits;•Helping to record any adverse events or symptoms that participants may experience while on study treatment.•Responsible for ensuring study is compliance with local and federal laws and regulations•Recruits and screens potential study participants and performs intake assessments•Creates and/or maintains all documents and records related to the study•Acts as a point of reference for study participants by answering questions and keeping them informed on the study progress•Manages the inventory of equipment and supplies related to the study and orders more as needed•Attends meetings, events and seminars in order to promote the study•Collects specimens and inputs data and patient information into electronic systems•Creates reports on each study, including notes on protocols, workload, data collection, and more