Clinical Research Associate I - Trials & Site Oversight

Mount Sinai Health System; United States; On-site; USD 55,000 - 75,000; Full time

Job summary

Mount Sinai Health System seeks a Clinical Research Associate I to monitor the clinical study lifecycle, with emphasis on site management, maintenance, and study closure across phases I–IV and post-marketing studies.

The role includes preparing critical documents, coordinating with investigators, maintaining the CTMF, tracking adverse events, and ensuring SOP/regulatory compliance. Degree required; 1–2 years in clinical research preferred.

Qualifications

• Bachelor's degree in life sciences or BSN.
• 1-2 years experience in clinical research.
• Experience in Phase I–IV studies desirable.

Responsibilities

• Monitor the clinical study lifecycle and site management.
• Prepare and edit essential study documents.
• Maintain CTMF and ensure regulatory compliance.
• Coordinate investigator meetings and site communications.
• Track adverse events and safety reports.
• Assist in budget tracking and grant payments.
• Contribute to data clarification and study closures.

Skills

Clinical research processes

Site management

Documentation accuracy

Communication

Education

Bachelor's degree in life sciences or BSN

Tools

CTMF systems

Job description

Mount Sinai Health System seeks a Clinical Research Associate I to monitor the clinical study lifecycle, with emphasis on site management, maintenance, and study closure across phases I–IV and post-marketing studies.

The role includes preparing critical documents, coordinating with investigators, maintaining the CTMF, tracking adverse events, and ensuring SOP/regulatory compliance. Degree required; 1–2 years in clinical research preferred.