Clinical Research Associate, Level II
Posted Aug 11
Posted Aug 11
This is a fully remote position, open to applicants in Mexico.
• Carry out site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensure adherence to protocols, data accuracy, and patient safety throughout the trial lifecycle.
• Work in collaboration with investigators and site personnel to ensure smooth execution of studies.
• Conduct data analysis and resolve queries to uphold the quality of clinical data.
• Assist in the preparation and evaluation of study documents, including protocols and clinical study reports.
• Bachelor's degree in a scientific or healthcare-related discipline.
• A minimum of 2 years of experience in the role of a Clinical Research Associate.
• Comprehensive understanding of clinical trial processes, applicable regulations, and ICH-GCP guidelines.
• Excellent organizational and communication abilities, with a keen eye for detail.
• Capability to work both independently and as part of a team in a fast-paced environment.
• Willingness to travel at least 70% of the time, both domestically and internationally, by air and car.
• Possession of a valid driver’s license.
• Legal eligibility to work in Mexico.
• Competitive base salary along with performance-related incentives.
• Health and wellness programs, including medical, dental, and vision coverage where applicable.
• Retirement and pension plans.
• Life insurance and disability coverage.
• Employee assistance programs and wellness resources.
• Opportunities for learning and development through structured training and career pathways.
Worldwide Clinical Trials
ICON plc
ICON plc
ICON plc
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