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ICON is seeking a Contract Senior Clinical Research Associate for a six-month position, responsible for conducting and overseeing clinical trials. The ideal candidate should have a strong background in clinical research, with at least three years of independent monitoring experience and a focus on compliance and data integrity.
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Job Summary
This 6-month contract role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
The successful candidate must ensure protocol compliance, data integrity, and patient safety throughout the trial process.
Candidates are expected to travel at least 80% of the time both internationally and domestically with a valid driver's license.
Matching Summary
Match Score: 75
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ICON is seeking a Contract Senior Clinical Research Associate for a six-month position, responsible for conducting and overseeing clinical trials. The ideal candidate should have a strong background in clinical research, with at least three years of independent monitoring experience and a focus on compliance and data integrity.
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Skills & Requirements
Must-have
Minimum 3 years independent monitoring experience
Valid driver's license required
Ability to travel at least 80% of the time
In-depth knowledge of ICH-GCP guidelines
Bachelor's degree in scientific or health-related field
Nice-to-have
Strong organizational and communication skills
Experience in study coordinator or nursing role
Ability to work independently in fast-paced environment
Attention to detail in complex medical data analysis
Key Requirements
Minimum 3 years independent monitoring
Bachelor's degree in scientific or health-related field
Valid driver's license
Knowledge of clinical trial processes and regulations