Clinical Research Coordinator II: Impactful Study Coordination

Myana; New York (NY); On-site; USD 60,000 - 90,000; Full time

Job summary

Mount Sinai Health System is seeking a Clinical Research Coordinator to coordinate and analyze clinical assessments and manage study data in a NY setting. The role involves preparing grant and IRB documents, coordinating consent, and mentoring junior coordinators.

A bachelor’s degree in sciences or related field and at least 2 years of clinical research experience are required. The position emphasizes collaboration with investigators and regulatory staff to ensure compliant protocol submissions,

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

Bachelors degree in sciences or related field

Job description

Mount Sinai Health System is seeking a Clinical Research Coordinator to coordinate and analyze clinical assessments and manage study data in a NY setting. The role involves preparing grant and IRB documents, coordinating consent, and mentoring junior coordinators.

A bachelor’s degree in sciences or related field and at least 2 years of clinical research experience are required. The position emphasizes collaboration with investigators and regulatory staff to ensure compliant protocol submissions,