Clinical Research Coordinator I - All of Us Research Study

Mount Sinai Health System • New York, NY

2d

About The Position

The Clinical Research Coordinator I participates in clinical research activities related to the All of Us study, an NIH initiative to enroll one million people across the United States to 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 study documents, including materials for the Institutional Review Board and Grants and Contracts Office, and performs other study-related activities as needed.

The Clinical Research Coordinator assists with daily clinical research study activities, participant education and coordination, database entry, specimen handling, and maintenance of accurate study records. The position requires a bachelor’s or master’s degree in science or a closely related field; no experience is required, although one year of research experience is preferred.

Requirements

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

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.
• Assist with clinical research activities, including answering phone calls, screening participants for eligibility, scheduling and coordinating study visits, and administering lifestyle questionnaires.
• Assist with IRB and Grants and Contracts Office applications as needed.
• Maintain source documents and subject files in accordance with hospital procedures.
• Ensure accurate and complete compilation of subject data through chart reviews.
• Perform other related duties as requested.

What This Job Offers

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