
Senior Clinical Research Associate – West Coast
Posted Oct 28

Posted Oct 28
This is a fully remote position, open to applicants in Washington.
• Conduct on-site or remote monitoring visits for Pre-Study, Initiation, Interim, and Close-Out phases.
• Ensure that investigational facilities and personnel are suitable for the execution of the study.
• Identify principal investigators and confirm their qualifications, resources, facilities, equipment, and staff adequacy.
• Provide training to investigational site personnel as needed.
• Assist in the preparation of regulatory and/or Ethics Committee submissions when relevant.
• Mentor and guide new team members.
• Carry out co-monitoring visits to evaluate the performance of junior staff.
• A degree from a College or University in Life Sciences or an equivalent combination of education, training, and experience.
• Significant on-site monitoring experience in phase 2/3 clinical trials.
• Preferably, experience with complex trials in oncology or rare diseases.
• Proficient in English with full working capability.
• Strong organizational skills with the ability to plan, multitask, and thrive in a fast-paced team environment.
• Excellent communication, collaboration, and problem-solving abilities.
• Willingness to travel nationally.
• Option for remote work availability.
• Engaging and collaborative team atmosphere.
• Opportunities for mentoring and training.
• Chance to contribute to pharmaceutical treatments that positively impact patients.
• A diverse and inclusive workplace culture.
• Opportunities for professional growth.
• A passionate and collaborative team of experts.
ICON plc
ICON plc
ICON plc
Worldwide Clinical Trials
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