Clinical Research Coordinator II: Trials, Data & Protocols

Mount Sinai; United States; On-site; USD 60,000 - 75,000; Full time

Job summary

Mount Sinai in the United States is seeking a Clinical Research Coordinator to coordinate the clinical assessments of study subjects, screen and evaluate participants, and assist in interpreting moderately complex clinical research data.

Under supervision, you will prepare grant applications, ensure IRB/GCO document submissions, obtain informed consent, mentor junior coordinators, and support protocol amendments and renewals of ongoing trials.

Qualifications

• Under minimal supervision, coordinates the clinical assessments and analyzes moderately complex clinical research data.
• Prepares grant applications and documents and assists in protocol submissions (IRB, Grants and Contracts Office).
• Obtains informed consent for studies enrolling vulnerable subjects and independently for other clinical studies.

Responsibilities

• Coordinate the clinical assessments of the study subjects including 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.
• Mentors Clinical Research Coordinators in training.
• Performs other related duties.

Skills

Clinical research coordination

Data analysis

Regulatory documentation

Grant applications

Informed consent

Mentoring

Education

Bachelor's degree in sciences or related field

Job description

Mount Sinai in the United States is seeking a Clinical Research Coordinator to coordinate the clinical assessments of study subjects, screen and evaluate participants, and assist in interpreting moderately complex clinical research data.

Under supervision, you will prepare grant applications, ensure IRB/GCO document submissions, obtain informed consent, mentor junior coordinators, and support protocol amendments and renewals of ongoing trials.