Clinical Research Coordinator I Attention-DeficitHyperactivity Disorder

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).

• 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.

• Bachelors or Masters degree in Science or closely related field (preferably in Psychology public health biology neuroscience)
• No experience required. One year of research experience preferred.

Preferred Qualifications:

• 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