Clinical Research Associate I: Trial Lifecycle & Site Ops

Mount Sinai Morningside; New York (NY); On-site; USD 59,000 - 82,000; Full time

Job summary

Mount Sinai Morningside Health System in New York, NY seeks a Clinical Research Associate I to monitor all aspects of clinical trials from site management to study closure. You will handle critical documents, maintain the CTMF, and support cross-functional teams across phases I–IV.

Qualifications include a Bachelor's degree in life sciences or BSN and 1–2 years in clinical research; Phase I–IV experience is highly desirable. Join a leading academic medical center in a collaborative environment.

Qualifications

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

Responsibilities

• Prepare and finalize critical study documents and templates (e.g., protocol, informed consent, investigator brochures).
• Monitor resources and reports to meet milestones on time and within budget.
• Maintain clinical study master file (CTMF) and ensure regulatory compliance.
• Assist CTM with site meetings, minutes, and ISF materials.
• Coordinate pre-study documentation and essential regulatory documents from investigator sites.

Skills

Clinical trial management

Documentation & compliance

Education

Bachelor's degree in life sciences or BSN

Job description

Mount Sinai Morningside Health System in New York, NY seeks a Clinical Research Associate I to monitor all aspects of clinical trials from site management to study closure. You will handle critical documents, maintain the CTMF, and support cross-functional teams across phases I–IV.

Qualifications include a Bachelor's degree in life sciences or BSN and 1–2 years in clinical research; Phase I–IV experience is highly desirable. Join a leading academic medical center in a collaborative environment.