Responsible for coordinating and performing study specific clinical and regulatory activities across multiple study protocols of different therapeutic areas and phases, in accordance with appropriate regulations, Standard Operating Procedures (SOPs), and study specific protocols/plans and processes

Principal Accountabilities:

1. Coordinates and implements the assigned protocols and recruit subjects to collect data from patient charts, medical records, interviews, questionnaires, diagnostic tests and other sources.
2. Ensures compliance with protocol guidelines and requirements of regulatory agencies, identifies problems and/or inconsistencies and monitors patients' progress to include documentation and reporting of adverse events, and recommends corrective action as appropriate.
3. Coordinates the development of forms, questionnaires and the application of research techniques, assists in writing procedure manuals, reviews journals, abstracts and scientific lite...