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 I to assist in daily activities of clinical research studies, obtain informed consent, and manage study information. You will help prepare grant documents for IRB and Grants offices and support regulatory filings.

Responsibilities include data collection, participant screening, consent coordination, and preparing for monitoring visits, with opportunities to engage in grant preparation and regulatory processes.

Qualifications

• Bachelor's or Master's degree in Science or a closely related field.
• No experience required; one year of research experience preferred.
• Industry-sponsored clinical trials preferred.
• Regulatory experience preferred.

Responsibilities

• Collects and records study data; inputs information into a database.
• Obtains informed consent under supervision and educates participants about study requirements.
• Assists in screening participants for eligibility and registering subjects with sponsoring agency; administers lifestyle questionnaires.
• Assists in preparing grant applications, IRB/GCO submissions and filings.
• Maintains source documents and subject files; ensures complete compilation of 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 understanding

Data collection

IRB knowledge

Regulatory experience

Education

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

Job description

Mount Sinai Morningside is seeking a Clinical Research Coordinator I to assist in daily activities of clinical research studies, obtain informed consent, and manage study information. You will help prepare grant documents for IRB and Grants offices and support regulatory filings.

Responsibilities include data collection, participant screening, consent coordination, and preparing for monitoring visits, with opportunities to engage in grant preparation and regulatory processes.