Senior Clinical Study Manager - Hybrid, 25% Travel

BioSpace; Armonk (NY); Hybrid; USD 110,000 - 179,000; Full time

Job summary

Regeneron is seeking a Clinical Study Associate Manager to join its Clinical Trial management team in a role that supports the Clinical Study Lead. You will oversee study planning, risk mitigation, documentation, vendor management, and drug forecasting across regions, while ensuring data quality and budget alignment.

This on-site with hybrid flexibility position is based in Armonk, NY, with up to 25% travel and collaboration with internal teams and CRO partners to deliver trials that impact

Qualifications

• Bachelor's Degree required with 4+ years of relevant industry experience.
• Data-driven and detail-oriented with ability to deliver on study activities.
• Knowledge of ICH/GCP and regulatory guidelines.

Responsibilities

• May lead/oversee planning and management of a clinical study in assigned region(s).
• Contributes to risk assessment and risk mitigation strategies.
• Oversees development of study documents and TMF/CTMS setup and maintenance.
• Oversees vendor engagement and study drug forecasting and accountability.
• Supports recruitment/retention strategies and site activation progress.
• Monitors data quality and supports budget management and CAPAs as needed.

Skills

Clinical ops

Vendor mgmt

ICH/GCP

Budget mgmt

MS Office/Trial systems

Education

Bachelor's Degree

Tools

IVRS/IWRS

EDC

TMF

Project

PowerPoint

Word

Excel

Job description

Regeneron is seeking a Clinical Study Associate Manager to join its Clinical Trial management team in a role that supports the Clinical Study Lead. You will oversee study planning, risk mitigation, documentation, vendor management, and drug forecasting across regions, while ensuring data quality and budget alignment.

This on-site with hybrid flexibility position is based in Armonk, NY, with up to 25% travel and collaboration with internal teams and CRO partners to deliver trials that impact