Job Description
As a Clinical Monitoring Associate II, you will be responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. This includes conducting remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols.
You will utilize data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices.
Collaboration is key in this role as you will work closely with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials.
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Responsibilities
* Conduct remote monitoring of trial sites to ensure compliance with regulatory requirements and clinical protocols.
* Utilize data analytics and risk-based monitoring techniques to identify potential issues and trends.
* Develop and implement tools, procedures, and processes to enhance quality monitoring and support clinical trial success.
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Requirements
* Bachelor's degree or equivalent combination of education, training, and experience.
* Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
* Excellent communication, presentation, and interpersonal skills.
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Benefits
This is an opportunity to work with a leading organization in the biopharmaceutical industry, where you will have the chance to make a real difference in the lives of patients and contribute to the advancement of medical knowledge.
As a member of our team, you will enjoy a comprehensive benefits package, including competitive salary, health insurance, retirement plan, and generous paid time off.