Clinical Research Coordinator II - ISM, Surgery

Mount Sinai; United States; On-site; USD 60,000 - 80,000; Full time

Job summary

Mount Sinai seeks a Clinical Research Coordinator to coordinate subject assessments and manage study data under supervision. You will assist in grant preparation, IRB submissions, and ensure thorough chart reviews for data integrity.

The role includes obtaining informed consent, supporting protocol submissions, and mentoring junior coordinators. A bachelor’s degree in sciences and 2 years of clinical research experience are required.

Qualifications

• Bachelor's degree in sciences or related field.
• 2 years of clinical research.

Responsibilities

• Coordinate the clinical assessments of study subjects, including screening and evaluation.
• Prepare grant applications and ensure IRB/GCO documents are submitted.
• Compile subject data through chart reviews for accuracy and completeness.
• Assist Principal Investigator and regulatory staff with protocol submissions and amendments.
• Obtain informed consent under supervision for studies enrolling vulnerable subjects and for genetic tests; independently consent for other studies.
• Mentor Clinical Research Coordinators in training.
• Perform other related duties as assigned.

Skills

Clinical coordination

IRB submissions

Data analysis

Informed consent

Education

Bachelor's degree in sciences or related field

Job description

Under minimal supervision, coordinates the clinical assessments of the study subjects; analyzes and assists in interpreting moderately complex clinical research data. Prepares grant applications and documents and assists in protocol submissions (for e.g., Institutional Review Board, Grants and Contracts Office).

• Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
• Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
• Prepares and ensures grant applications, IRB/GCO documents are submitted.
• Ensures accurate and complete compilation of subject data through chart reviews.
• Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials.
• Obtains informed consent under supervision of the Principal Investigator, Clinical Research Manager, or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects, and for studies involving genetic tests.
• Independently obtains informed consent for other clinical studies.
• Mentors Clinical Research Coordinators in training.
• Performs other related duties.

• Bachelors degree in sciences or related field.
• 2 years of clinical research

Non-Bargaining Unit, 862 - Surgery - ISM, Icahn School of Medicine