Clinical Research Coordinator I-OB/GYN

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

Job summary

Mount Sinai seeks a Clinical Research Coordinator to support daily activities of clinical research studies, obtain informed consent, and manage study data. The role includes assisting with grant applications, IRB/GCO filings, and maintaining study documents.

Responsibilities include data entry, screening participants for eligibility, registering subjects with sponsoring agencies, and coordinating specimen handling.

Qualifications

• Collects and records study data and inputs information into the database.
• Obtains informed consent under minimal supervision and educates participants about study requirements.
• Assists in screening participants for eligibility and registering subjects with sponsoring agency.

Responsibilities

• Maintains source documents and subject files according to hospital procedures.
• Prepares for monitoring visits and submits filings for IRB/GCO.
• Secures and ships clinical specimens as required by the protocol.
• Performs other related duties as needed.

Skills

Informed consent

Data collection

Study coordination

IRB knowledge

Education

Bachelor's degree in Science

Master's degree in Science

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).

1. Collects and records study data. Inputs all information into database.

2. Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.

3. 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.

4. Assists in preparing grant applications, IRB/GCO for submission and filings.

5. Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews.

6. Secures, delivers and ships clinical specimens as required by the protocol.

7. Prepares for monitoring visits.

8. Performs other related duties.

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

Non-Bargaining Unit, 843 - Obs/Gyn Reproductive Science - ISM, Icahn School of Medicine, OBGYN