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About the role

Overview: In this role you support clinical dermatology research under supervision, handling consent, data collection, and study documentation. You work with the PI and senior staff to advance clinical studies and prepare regulatory submissions. You help ensure data quality and compliance while engaging with participants and coordinating study activities. This is an opportunity to contribute to translational dermatology research within a renowned academic health system.
Responsibilities: Obtain informed consent and screen participants for eligibility Collect, organize and maintain study data and source documents Assist with regulatory submissions and grant-related tasks Support data analysis and preparation of publications/presentations Coordinate with sponsors and perform study-related communications May ship specimens and assist in regulatory site visits Maintain confidentiality and compliance with policies
Key requirements: Bachelor degree in science or related field or equivalent research experience 0-2 years in research or human subjects experience Knowledge of informed consent processes and data handling Experience supporting regulatory documentation and study coordination Strong organizational and communication skills Attention to detail Reliable and collaborative teamwork Effective written and verbal communication Informed consent administration Participant screening and data collection Source document management

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JOB OVERVIEW

Experience level

Senior

Location

Brooklyn, NY

Occupation

Clinical Research Coordinators

Industry

Research and Development in the Physical, Engineering, and Life Sciences

Posted

today

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