Clinical Study Associate Manager

Regeneron Pharmaceuticals, Inc.

Armonk (NY)

On-site

USD 110,000 - 140,000

Full time

14 days+
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Job summary

Regeneron Pharmaceuticals is seeking a Clinical Study Associate Manager to support clinical trial delivery within a global management team. The role involves oversight of regional study planning, vendor management, study documentation, and system setup (CTMS, TMF), with site activation and recruitment responsibilities.

The candidate will contribute to risk mitigation, feasibility assessments, and inspection readiness, ensuring adherence to GxP and ICH/GCP guidelines while managing budgets and

Qualifications

  • Bachelor's degree required.
  • 4+ years in clinical operations.
  • Proficiency with trial management systems (EDC, TMF, IVRS).
  • Budget awareness.
  • Vendor management experience.
  • Knowledge of GxP and ICH/GCP guidelines.

Responsibilities

  • Oversee regional study planning and vendor management.
  • Manage study documentation and CTMS/TMF setup.
  • Site activation, recruitment, data quality, and study close-out.
  • Contribute to risk mitigation, feasibility, and inspection readiness.

Skills

Vendor management
Budget awareness
GxP knowledge
EDC familiarity
TMF familiarity
IVRS familiarity

Education

Bachelor's degree

Tools

EDC
TMF
IVRS

Job description

Role

Clinical Study Associate Manager supporting clinical trial delivery within Regeneron's global management team.

Responsibilities
  • oversee regional study planning, vendor management, study documentation, system setup (CTMS, TMF), site activation, recruitment, data quality, budget, and study close-out activities
  • contribute to risk mitigation, feasibility, and inspection readiness
Requirements
  • Bachelor's degree
  • 4+ years in clinical operations
  • proficiency in trial management systems (EDC, TMF, IVRS)
  • budget awareness
  • vendor management experience
  • knowledge of GxP and ICH/GCP guidelines
HighValue
  • clinical trial management, study documentation, vendor oversight, data quality, budget management
  • experience with biologics or small molecules is implied but not explicitly stated
WorkSetup
  • On-site with travel (~25%) in Armonk, NY; Warren, NJ; or Cambridge, MA.
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