Clinical Research Assistant-CCTO

Location: Upper East Side

Position Summary

Under direction, the Clinical Research Assistant coordinates the data management of clinical research studies.

Responsibilities

• Responsible for data management of clinical research studies in compliance with federal regulations, GCP guidelines, and internal policies.
• Responsible for the accurate and timely collection, compilation, and entry of data for clinical trials, including reviewing patient charts, existing databases, and other sources.
• Works closely with the research team on data input and data entry query resolution.
• Ensures data quality and integrity throughout the life of the study.
• Maintains complete research charts for assigned caseload of subjects.
• Completes all required case report forms and resolves all outstanding queries in a timely manner.
• Generates study‑specific tools to ensure protocol compliance.
• Participates in research team meetings.
• Performs other job‑related duties as required.

Education

• High School Diploma required.
• Bachelor’s degree preferred.
• Some relevant research experience.

Knowledge, Skills, and Abilities

• Strong communication and interpersonal skills; ability to interact with multiple constituencies and exercise “people skills.”
• Proficiency with MS Office Suite and database applications.
• Organizational skills and close attention to detail.
• Critical thinking and analytical skills.
• Ability to multi‑task and prioritize in a fast‑paced environment.
• Ability to remain focused despite frequent interruptions.
• Ability to treat confidential information with utmost discretion.
• Professional standards of appearance, presentation, and demeanor.
• Effective collaboration with departmental faculty, staff, and institutional representatives.

Pay

• Salary range: $24.29 – $27.09 per hour.
• Exemption status: Non‑Exempt.

Schedule

• Work days: Monday‑Friday.
• Weekly hours: 35.00.