Clinical Research Assistant-CCTO

at  Weill Cornell Medicine

TITLE: CLINICAL RESEARCH ASSISTANT-CCTO

Title: Clinical Research Assistant-CCTO
Location: Upper East Side
Org Unit: Leukemia/ MPN
Work Days: Monday-Friday
Exemption Status: Non-Exempt

Salary Range: $22.11 - $25.99

• As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role when Hired for NYC Offices

POSITION SUMMARY

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

EDUCATION

• High School Diploma

EXPERIENCE

Bachelor’s degree preferred.
Some relevant research experience.

KNOWLEDGE, SKILLS AND ABILITIES

• Demonstrated strong communication and interpersonal skills; demonstrated ability to interact with multiple constituencies and exercise “people skills”.
• Demonstrated proficiency with MS Office Suite and database applications.
• Demonstrated organizational skills and ability to pay close attention to detail.
• Demonstrated critical thinking and analytical skills.
• Demonstrated ability to multi-task and prioritize in a fast-paced environment.
• Demonstrated ability to remain focused despite frequent interruptions.
• Ability to treat confidential information with utmost discretion.
• Ability to exercise standards of professionalism, including appearance, presentation and demeanor.
• Demonstrated ability to work effectively in a collaborative manner with all departmental faculty and staff, as well as other institutional representatives.

• 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 timely manner.
• Generates study-specific tools to ensure protocol compliance.
• Participates in research team meetings.
• Performs other job related duties as required.