Novartis

Novartis

Clinical Research Associate (CRA) Manager

Field Non-Sales (USA)

Sponsorship not specifiedDetected 80 days ago
Data AnalysisComplianceProject ManagementNegotiationClinical TrialsClinical ResearchResearchLeadershipCommunicationCollaborationProblem SolvingMentoringGxP

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odds of building a lasting career here

40Risky
Cap-exempt (no lottery)0
Sponsors this role90
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70

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Files H-1B transfers

1 transfer filing in the last year, covering 1 worker. Median labor-condition decision: 7 days. An employer that already files transfers is one that can take over an existing H-1B.

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About the role

  • Ensure monitoring excellence through targeted coaching, training, and co-monitoring activities.
  • Clinical Research Associate (CRA) Manager
  • Continental United States (field-based; candidates should be located near a major airport)

Responsibilities

  • Lead, coach, and develop a team of Clinical Research Associates across multiple clinical development programs.
  • Drive performance against quality, productivity, enrollment, and monitoring delivery objectives.
  • Build team capabilities to support successful execution of Phase I through Phase IV clinical trials.
  • Collaborate with cross-functional partners to support enrollment, data quality, and issue resolution.
  • Manage performance, development planning, and retention of a high-performing Clinical Research Associate organization.
  • Support audit and inspection readiness, including corrective and preventive action implementation and follow-up.
  • Partner on resource planning strategies to balance workload, capacity, and business priorities.
  • Proven experience leading, coaching, and developing people and teams in a clinical research environment. Demonstrated ability to manage people, performance, productivity, quality, and delivery objectives.
  • Experience building effective partnerships with cross-functional stakeholders and clinical trial sites.

Requirements

  • Strong understanding of clinical drug development, trial monitoring, and study execution processes.
  • Strong knowledge of Good Clinical Practice, regulatory requirements, and clinical trial compliance standards.
  • Minimum 7+ years of experience planning, executing, and monitoring clinical trials across multiple phases of development.

Skills

  • Excellent project management, prioritization, communication, and problem-solving skills.
  • Fluent in both written and spoken English; Strong communication skills, both written and oral.

Compensation

  • $145,600.00 - $270,400.00

Benefits

  • A degree in scientific or health discipline preferable; 4-year degree plus relevant, related healthcare experience required).
  • Budget Management, Clinical Research, Clinical Study Reports, Clinical Trials, Collaboration, Data Analysis, Health Sciences, People Management, Regulatory Compliance

This listing is sourced directly from Novartis's careers page and normalized into a canonical job model.