Senior Clinical Research Coordinator – Trials & Data

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

Job summary

Mount Sinai Health System in New York City seeks a Clinical Research Coordinator to coordinate the clinical assessments of study subjects and contribute to the interpretation of moderately complex research data. You will prepare grant applications and assist with protocol submissions to IRB and Grants offices.

The role includes obtaining informed consent, mentoring coordinators, and ensuring accurate data compilation through chart reviews, with opportunities to support protocol amendments and

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.

Skills

Clinical Research

Education

Bachelor's degree in sciences or related field

Job description

Mount Sinai Health System in New York City seeks a Clinical Research Coordinator to coordinate the clinical assessments of study subjects and contribute to the interpretation of moderately complex research data. You will prepare grant applications and assist with protocol submissions to IRB and Grants offices.

The role includes obtaining informed consent, mentoring coordinators, and ensuring accurate data compilation through chart reviews, with opportunities to support protocol amendments and