Clinical Research Coordinator I-Neurosurgery

Mount Sinai; United States; On-site; USD 55,000 - 75,000; Full time

Job summary

Mount Sinai Health System is seeking a Clinical Research Coordinator I-Neurosurgery to assist in daily clinical research activities. You will collect and record study data, obtain informed consent, and maintain study documentation in accordance with hospital procedures.

You will support grant applications, ensure regulatory submissions (IRB/Grants & Contracts), ship specimens as needed, and help screen participants for eligibility under supervision, enabling high-quality research in neurosurgery.

Qualifications

• Bachelor's or Master's degree in Science or closely related field.
• No experience required. One year of research experience preferred.

Responsibilities

• Collects and records study data. Inputs all information into database.
• Obtains informed consent under minimal supervision and educates participants regarding study requirements.
• Assists in activities related to clinical research studies including screening participants for eligibility and registering subjects with sponsor.
• Assists in preparing grant applications, IRB/GCO submissions and filings.
• Maintains source documents and subject files per hospital procedures; ensures accurate data through chart reviews.
• Secures, delivers and ships clinical specimens as required by the protocol.
• Performs other related duties.

Skills

MS Excel

MS Word

Microsoft Access

Outlook

SSPS/SAS

Education

Bachelor's or Master's degree in Science or closely related field

Job description

Clinical Research Coordinator I-Neurosurgery

Job Description

The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office).

Responsibilities

• Collects and records study data. Inputs all information into database.
• Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
• Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires.
• Assists in preparing grant applications, IRB/GCO for submission and filings.
• Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews.
• Secures, delivers and ships clinical specimens as required by the protocol.
• Performs other related duties.

Qualifications

• Bachelors or Masters degree in Science or closely related field.
• No experience required. One year of research experience preferred.

Required Skills

• MS Excel
• MS Word
• Microsoft Access
• Outlook
• SSPS/SAS

Equal Opportunity Employer

The Mount Sinai Health System is an equal opportunity employer, complying with all applicable federal civil rights laws. We do not discriminate, exclude, or treat individuals differently based on race, color, national origin, age, religion, disability, sex, sexual orientation, gender, veteran status, or any other characteristic protected by law. We are deeply committed to fostering an environment where all faculty, staff, students, trainees, patients, visitors, and the communities we serve feel respected and supported. Our goal is to create a healthcare and learning institution that actively works to remove barriers, address challenges, and promote fairness in all aspects of our organization.