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Job Description & How to Apply Below
Overview Elevate your career as a Lead Clinical Research Associate, focusing on site management in clinical studies. This role involves both in office and remote monitoring to ensure compliance and safety throughout the research process. We are seeking an experienced individual to oversee site qualification, site initiation, and interim monitoring. You will utilize your knowledge of ICH/GCP Guidelines and regulatory requirements to maintain data integrity while collaborating with site teams.
The responsibility also includes effective problem resolution and communication of responsible issues to the project team. Enhance your skills in clinical monitoring and ensure compliance in an agile research environment.
Key Responsibilities Perform site initiation and close-out visits
Evaluate site performance and communicate issues
Conduct source document reviews and data verification
Ensure the informed consent process is followed
Manage project timelines and site-level activities
Requirements Bachelor's degree in a related field
Strong knowledge of GCP/ICH Guidelines
Excellent computer and communication skills
Up to 75% travel availability
Experience mentoring junior CRAs
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Position Requirements
10+ Years
work experience
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