Clinical Research Coordinator I — Study Data & Compliance

Mount Sinai; United States; On-site; USD 52,000 - 68,000; Full time

Job summary

Mount Sinai seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, collect and organize study data, and assist with grant-related documents.

No experience required; a Bachelor's or Master's in science is required. The role includes data entry, screening participants, preparing IRB/GRANT submissions, and coordinating specimen handling.

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 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.

Education

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

Job description

Mount Sinai seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, collect and organize study data, and assist with grant-related documents.

No experience required; a Bachelor's or Master's in science is required. The role includes data entry, screening participants, preparing IRB/GRANT submissions, and coordinating specimen handling.