Clinical Research Coordinator II: Trials & Data

Mount Sinai; New York (NY); On-site; USD 66,000 - 98,000; Full time

Job summary

The Mount Sinai Health System seeks a coordinator to supervise clinical assessments and assist in managing moderately complex clinical data. You will help prepare grant applications and IRB/Grants and Contracts Office submissions, ensure data integrity through chart reviews, and support protocol submissions and amendments.

Responsibilities include obtaining informed consent under supervision and, for some studies, independently, while mentoring junior coordinators and performing related duties

Qualifications

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

Responsibilities

• 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.

Education

Bachelor's degree in sciences or related field

Job description

The Mount Sinai Health System seeks a coordinator to supervise clinical assessments and assist in managing moderately complex clinical data. You will help prepare grant applications and IRB/Grants and Contracts Office submissions, ensure data integrity through chart reviews, and support protocol submissions and amendments.

Responsibilities include obtaining informed consent under supervision and, for some studies, independently, while mentoring junior coordinators and performing related duties