
Clinical Trials Manager
3 days ago
This role involves coordinating various aspects of clinical monitoring and site management. The successful candidate will have a strong understanding of medical/therapeutic area knowledge, excellent critical thinking skills, and the ability to manage risk-based monitoring concepts.
About the Role- The Senior Clinical Research Associate will be responsible for performing and coordinating all aspects of clinical monitoring and site management.
- This includes assessing protocol and regulatory compliance, managing required documentation, and developing collaborative relationships with investigational sites.
- The role also involves monitoring investigator sites using a risk-based approach, identifying site process failures, and implementing corrective actions.
- The Senior Clinical Research Associate must ensure that trials are conducted in accordance with approved protocols, ICH-GCP guidelines, and applicable regulations.
The ideal candidate will have a Bachelor's degree in a life sciences-related field or equivalent experience, and at least 3 years of clinical research monitoring experience, including 2 years in Oncology.
BenefitsThis role offers opportunities for professional growth and development, as well as a competitive salary and benefits package.
Working EnvironmentThe Senior Clinical Research Associate will work from home and be required to travel up to 80% of the time, including overnight stays.
Why Join Us?We value our employees' health and well-being and offer a range of benefits to support their physical and mental health.
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