Clinical Research Coordinator I- Pulmonary

Mount Sinai; United States; On-site; USD 40,000 - 60,000; Full time

Job summary

Mount Sinai is seeking a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and manage study data. The role includes assisting in grant preparation, IRB submissions, and coordinating with sponsors.

The candidate will collect and input data, maintain subject files, and help screen participants for eligibility. No experience is required, though 1 year of research experience is preferred.

Qualifications

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

Responsibilities

• Assist daily activities of clinical research studies and obtain informed consent.
• Collect, maintain and organize study information; input data into database.
• Prepare grant applications and documents (e.g., IRB, Grants and Contracts Office).
• Secure, deliver and ship clinical specimens as required by the protocol.
• Prepare for monitoring visits and maintain source documents/subject files.
• Screen participants for eligibility and assist in coordinating with sponsors.
• Perform other related duties.

Education

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

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).

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.

Prepares for monitoring visits.

Performs other related duties.

Bachelors or Masters degree in Science or closely related field.

No experience required. One year of research experience preferred.