Psychiatry Clinical Research Coordinator (Entry Level)

Mount Sinai Morningside; New York (NY); On-site; USD 59,000 - 74,000; Full time

Job summary

Mount Sinai Morningside is seeking a Clinical Research Coordinator to assist in the daily activities of clinical research studies, obtain informed consent, and collect, maintain and organize study information. The role supports the preparation of grant applications and documents for IRB and Grants and Contracts.

You will collect and record data, enter information into databases, help with screening, enrollment, and scheduling, maintain source documents, secure specimens, and assist with

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 information into database.
• Obtains informed consent under 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.

Skills

Informed consent

Data collection

Data entry

Education

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

Job description

Mount Sinai Morningside is seeking a Clinical Research Coordinator to assist in the daily activities of clinical research studies, obtain informed consent, and collect, maintain and organize study information. The role supports the preparation of grant applications and documents for IRB and Grants and Contracts.

You will collect and record data, enter information into databases, help with screening, enrollment, and scheduling, maintain source documents, secure specimens, and assist with