
Senior Clinical Research Associate – East Coast
Posted Oct 28

Posted Oct 28
This is a fully remote position, open to applicants in New York.
• Conduct Pre-Study, Initiation, Interim, and Close-Out monitoring visits, either on-site or remotely.
• Ensure that facilities and personnel at investigational sites are sufficient for the execution of the study.
• Identify and assess investigators while confirming their qualifications, resources, facilities, equipment, and staff throughout the duration of the study.
• Provide training to investigational site personnel as needed.
• Assist in the preparation of regulatory and/or Ethics Committee submissions when necessary.
• Mentor and train new team members.
• Carry out co-monitoring visits to evaluate the performance of junior staff.
• A College/University degree in Life Sciences or a comparable combination of education, training, and experience.
• Significant on-site monitoring experience in phase 2/3 clinical trials.
• Preferably, experience with complex clinical trials in oncology or rare diseases.
• Full working proficiency in English is required.
• Ability to plan, prioritize, and work effectively in a fast-paced team environment.
• Strong communication, collaboration, and problem-solving abilities.
• Willingness to travel nationally as needed.
• Opportunity for remote work.
• Work alongside a dedicated and collaborative team of experts.
• A diverse and inclusive workplace where every individual's voice is valued.
ICON plc
ICON plc
ICON plc
Worldwide Clinical Trials
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