Clinical Research Coordinator II: Study Data & Protocol

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

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.