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NYU Langone Health · 8 hours ago

Clinical Research Associate - Surgery CSTAR - Based in Long Island and Manhattan

New York, NY

Full-time

Onsite

Entry Level

$47K/yr - $64K/yr

2+ years exp

NYU Langone Health is a leading medical institution committed to improving human health through education, research, and patient care. The Clinical Research Associate will conduct independent clinical research, interact with human subjects, and maintain research data, while also supporting trial activities and compliance with protocols.

EducationHealth CareHospitalMedicalNon Profit

Growth Opportunities

Responsibilities

Performs in-person and over-the-phone participant recruitment

Performs data collection over the phone, by email or in dialysis centers, in-patient, and out-patient settings (or other clinical settings)

Performs in-person and over-the-phone follow-up of participants who are enrolled in clinical trials and cohort studies

Conducts chart abstractions to ascertain clinical data

Administers behavioral, exercise and other interventions in clinical settings. Reports enrollment, follow-up, and retention rates for clinical trials and cohort studies

Prepares and maintains Standard Operating Procedures(SOPs) for clinical trials and cohort studies

Performs specimen processing and storage

Maintains study databases by entering, cleaning, and verifying data for accuracy and completeness

Coordinates communication between study sites, clinical staff, and research team members to ensure protocol adherence and timely data collection

Participates in study team meetings and contributes to protocol development, recruitment strategies, regulatory submissions, and process improvement discussions

Assists in the development and pilot testing of study instruments, surveys, and data collection tools

Prepares study materials such as recruitment flyers, participant packets, and consent forms

Schedules and documents study visits, maintaining detailed logs for tracking participant flow and study progress

Assists in the preparation of reports, abstracts, posters, and manuscripts for presentations and publications

Ensures compliance with Good Clinical Practice (GCP) and institutional policies related to participant safety, confidentiality, and data management

Monitors study supplies and coordinates with laboratory and clinical teams to ensure proper inventory and equipment maintenance

Assists with quality assurance activities, including source document verification and internal audits

Supports grant and budget tracking, including study reimbursements and invoicing for multicenter projects

After a period of time working with the research team, the candidate will be expected to train newly hired Research Associates, graduate students, and postdoctoral fellows in the study design, data collection, blood processing technique, and other aspects of the research

Qualification

Clinical researchData collectionClinical Practice (GCP)Biomedical researchParticipant recruitmentCommunication skillsTeam collaborationProblem-solving