As a Clinical Research Associate II, you will be responsible for conducting on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.
Key Responsibilities:
* Conduct on-site and remote monitoring of clinical research studies
* Develop tools, procedures, and processes to ensure quality monitoring
* Provide guidance and support to clinical research teams
* Maintain accurate and timely documentation of monitoring activities
* Collaborate with cross-functional teams to ensure successful trial execution
You will work closely with clinical research teams to ensure the success of clinical trials. This includes developing and implementing monitoring plans, managing site-level activities, and ensuring regulatory compliance.
The ideal candidate will have a bachelor's degree in a related field and a minimum of 5 years of experience in clinical research monitoring. In-depth knowledge of clinical trial processes and regulations is essential, as well as strong analytical and problem-solving skills.