• Pre-Screening• Screening and Informed consent• Running the clinical trial• Ensure all protocols and procedures are followed• Monitor subject safety throughout the trial• Coordinate communication between researchers, sponsors, and subjects• Coordinating with study participants to ensure they understand their participation requirements and any possible risks or benefits of the study• Reviewing study protocols, progress reports, and interim results to ensure that studies are being conducted according to design and that results are accurately recorded• Reviewing reports from Institutional Review Boards (IRBs) to ensure that study protocols are in compliance with regulations• Coordinating with investigators to ensure that all research activities are carried out in accordance with protocols and approved by ethics boards• Maintaining accurate records of study data such as lab results and clinical findings• Preparing budgets and managing budgets for clinical trials• Preparing and sending correspondence to investigators regarding study procedures and requirements• Scheduling appointments for study participants to visit clinical research facilities for examinations• Submitting study completion reports to ethics boards or institutional review boards

Business Management• Oversee practice processes• Business Development Strategies• Monitor Human Resource System and Ensure Compliance• Maintaining Positive and Trust-Based Relations With Employees, Business Partners, and Clients• Assessing, Managing, and Resolving Problematic Developments and SituationsFinance Management• Directing Financial Planning and Strategy• Analyzing and Reporting On Financial Performance

Locum work