Overall Purpose:
As a Study Monitor, you will play a pivotal role in overseeing the progress of clinical and application research trials. You will ensure that all studies are conducted, recorded, and reported in compliance with protocols, SOPs, ICH-GCP, and applicable regulatory requirements. You will provide a global evaluation of all investigations commissioned and executed, acting as the crucial link between investigators and research personnel.
Why Join ?
I am seeking an exceptional individual who brings innovative ideas, a positive attitude, and a professional demeanor. You will thrive in this dynamic environment where your expertise will drive clinical research excellence. As a key member of the Clinical and Application Research Team, you will play a critical role in advancing our cutting-edge clinical trials and ensuring the highest standards of quality and compliance.
Key Responsibilities:
1. Study Oversight: Oversee clinical trial progress, ensuring compliance with regulatory standards and protocols.
2. Document Management: Prepare and manage essential study documentation, ensuring compliance from start-up to close-out.
3. Data Verification: Ensure accurate patient data recording across multiple investigations.
4. Investigator Training: Conduct on-site training, providing motivation and guidan...