Clinical Research Coordinator I - All of Us Research Study

Mount Sinai Health Systems • New York, NY

3d • $58,661 - $73,530

About The Position

The Clinical Research Coordinator I participates in clinical research activities for the All of Us study, an NIH initiative to enroll one million people across the U.S. to help build a diverse health database. The coordinator obtains informed consent, collects and processes biospecimens, performs some clinical assessments, and collects, maintains, and organizes study information. The role also assists with preparing documents for the Institutional Review Board and Grants and Contracts Office, along with other study-related activities as needed.

The position supports the daily activities of clinical research studies, including participant education and coordination, data collection and documentation, specimen handling, and maintenance of source documents and subject files in accordance with hospital procedures. The Mount Sinai Health System describes its workplace as committed to inclusion, collaboration, fairness, continuous learning, and outstanding patient care.

Requirements

• Bachelor’s or master’s degree in science or a closely related field.
• No experience is required.
• Strong communication and organizational skills.
• Ability to work effectively, communicate clearly, and accomplish goals.
• Attention to detail and ability to manage time and multitask in a fast-paced environment.
• Effective interpersonal skills, including the ability to establish working relationships and collaborate with employees at all levels.
• Ability to foster cooperation in others.

Nice To Haves

• One year of research experience preferred.
• Proficiency in Microsoft Office Suite.
• Background in clinical research or a closely related field.
• Passion for patient care and clinical research.
• Bilingual in Spanish (preferred but not required).

Responsibilities

• Obtain informed consent and educate participants about study requirements.
• Collect and record study data and enter information into a database.
• Collect, process, deliver, and ship clinical specimens as required by the protocol.
• Support clinical research activities, including answering phone calls, screening participants for eligibility, scheduling and coordinating study visits, and administering lifestyle questionnaires.
• Assist with Institutional Review Board and Grants and Contracts Office applications as needed.
• Maintain source documents and subject files in accordance with hospital procedures.
• Review charts to ensure accurate and complete compilation of subject data.
• Perform other related duties as requested.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level