Senior Clinical Research Associate responsible for site management and monitoring for Karius. Ensures compliance with protocols and GCP guidelines during clinical trials.
About the role
- Senior Clinical Research Associate overseeing the quality and compliance of clinical trial sites for BMS. Conducting site visits, monitoring adherence to regulations, and collaborating with stakeholders.
Responsibilities
- Conduct site qualification, initiation, routine monitoring, and close-out visits across all trial phases
- Maintain the ethical and scientific integrity of clinical trials
- Monitor site adherence to ICH GCP and local regulations
- Cultivate and sustain effective relationships with internal and external partners
- Prepare and submit written reports in a timely and accurate manner
- Identify and assess potential Investigators and their sites
- Perform timely site closure activities.
Requirements
- Bachelor’s degree required, preferably within life sciences or equivalent
- Valid driver’s license (as locally required)
- At least 5 years of monitoring experience
- Extensive experience in all aspects of the role
- Knowledge of clinical research processes, regulations, and methodology
- Working knowledge of ICH/GCP Guidelines and applicable local laws
- Analytical thinking/critical thinking skills.
Benefits
- Competitive benefits, services, and programs for pursuing goals at work and in personal lives.
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Tech skills
Location requirements
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