Clinical Research Coordinator II — Trials & Data Analysis

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

Job summary

Mount Sinai Morningside in New York seeks a Clinical Research Coordinator to coordinate clinical assessments, analyze moderately complex data, and assist with protocol submissions. Under supervision, you will obtain informed consent, monitor study subjects, and support grant applications and regulatory documents.

This role requires a bachelor's degree in sciences and at least two years in clinical research.

Qualifications

• Bachelor's degree in sciences or related field.
• 2 years of clinical research experience.
• Experience with protocol submissions and IRB processes preferred.

Responsibilities

• Analyzes moderately complex clinical research data and assists in interpretation.
• Coordinates clinical assessments of study subjects including screening and evaluation.
• Prepares and submits grant applications and IRB/GCO documents.
• Ensures complete compilation of subject data through chart reviews.
• Assists PI and regulatory staff with protocol submissions and amendments.
• Obtains informed consent under supervision for studies enrolling vulnerable subjects and those involving genetic tests.
• Mentors Clinical Research Coordinators in training.

Skills

Clinical research

Data analysis

Education

Bachelor's degree in sciences or related field

Job description

Mount Sinai Morningside in New York seeks a Clinical Research Coordinator to coordinate clinical assessments, analyze moderately complex data, and assist with protocol submissions. Under supervision, you will obtain informed consent, monitor study subjects, and support grant applications and regulatory documents.

This role requires a bachelor's degree in sciences and at least two years in clinical research.