Entry-Level Clinical Research Coordinator

Mount Sinai; United States; On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Healthcare benefits

Job summary

Mount Sinai is seeking a Clinical Research Coordinator to assist in daily activities of clinical research studies, obtain informed consent, and manage study information. Responsibilities include data entry, screening, and supporting grant and IRB submissions.

The role involves maintaining records, coordinating with sponsors, and preparing for monitoring visits; a science-related degree is required with no experience or minimal experience preferred.

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 in the database.
• Obtains informed consent under minimal supervision and educates participants.
• Screening participants for eligibility; registering subjects with sponsoring agency; administering lifestyle questionnaires.
• Supports grant applications and IRB/GCO submissions.
• Maintains source documents and subject files; performs chart reviews.
• Secures, delivers and ships clinical specimens per protocol.
• Prepares for monitoring visits.
• Performs other related duties.

Skills

Informed consent

Data collection

Study coordination

Communication

Education

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

Job description

Mount Sinai is seeking a Clinical Research Coordinator to assist in daily activities of clinical research studies, obtain informed consent, and manage study information. Responsibilities include data entry, screening, and supporting grant and IRB submissions.

The role involves maintaining records, coordinating with sponsors, and preparing for monitoring visits; a science-related degree is required with no experience or minimal experience preferred.