Clinical Research Coordinator I - Attention-Deficit/Hyperactivity Disorder

Mount Sinai Health System • New York, NY

1d

About The Position

The Icahn School of Medicine at Mount Sinai is seeking a highly motivated Clinical Research Coordinator I (CRC I) to support an innovative, patient-centered research study focused on treatment strategies for Attention-Deficit/Hyperactivity Disorder (ADHD) in school-age youth. This study evaluates whether nonstimulant medications are as effective and acceptable as stimulant medications when used as first-line treatment. The research emphasizes real-world clinical decision-making, heterogeneity of treatment effects, and long-term outcomes, with active engagement from a partnership board including parents, clinicians, teachers, and ADHD advocates. The CRC I will be responsible for coordinating day-to-day study operations, supporting participant engagement, and ensuring high-quality data collection across a longitudinal study design. The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office).

Requirements

• Bachelors or Masters degree in Science or closely related field (preferably in Psychology, public health, biology, neuroscience)
• No experience required.

Nice To Haves

• One year of research experience preferred.
• Prior experience in clinical research or healthcare
• Experience working with pediatric or behavioral health populations
• Experience with REDCap or other clinical data systems
• Knowledge of IRB processes and Good Clinical Practice (GCP)
• Bilingual in English and Spanish

Responsibilities

• Coordinate daily operations of a clinical research study involving pediatric participants with ADHD
• Recruit, screen, consent, and enroll study participants and their families
• Schedule and manage study visits
• Administer standardized assessments and surveys
• Maintain accurate and timely data entry in electronic data capture systems (e.g., REDCap)
• Ensure compliance with Institutional Review Board (IRB) requirements and Good Clinical Practice (GCP) guidelines
• Attend research team meetings
• Assist in preparing reports, study documentation, and presentations
• Complete miscellaneous duties as assigned
• Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires.
• Maintains source documents and subject files in accordance with hospital procedures.
• Ensures accurate and complete compilation of subject data through chart reviews.
• Secures, delivers and ships clinical specimens as required by the protocol.
• Prepares for monitoring visits.
• Performs other related duties.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 5,001-10,000 employees