Entry-Level OB/GYN Clinical Research Coordinator

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

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.