Remote Clinical Trial Manager II: Lead Site & Risk Oversight

Syneos Health, Inc.

Ciudad de México

Hybrid

MXN 900.000 - 1.300.000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Syneos Health, Inc. is seeking a Clinical Trial Manager II for Ciudad de Mexico with remote work options. You’ll oversee site management, monitoring, and data integrity across studies, coordinating with cross-functional teams.

The role emphasizes patient safety, regulatory compliance, and risk mitigation to ensure trial success. The incumbent will manage RA/monitoring activities, contribute to risk assessments, and drive timelines and budgets while supporting protocol execution and sponsor

Qualifikationen

  • Bachelor’s degree or RN in a related field or equivalent.
  • Experience leading clinical monitoring and site management.
  • Knowledge of GCP/ICH guidelines and regulatory requirements.

Aufgaben

  • Oversee site management and monitoring activities from activation to closeout.
  • Collaborate with functional teams to meet milestones and timelines.
  • Identify risks with risk-based monitoring and implement mitigations.
  • Manage budgets, contracts, and scope with sponsors and sites.
  • Develop study tools and templates, including the CMP/SMP.
  • Provide training to study teams on protocols, CRFs, and data plans.

Kenntnisse

Team leadership
Risk-based monitoring
Budget management
GCP/ICH knowledge
Cross-functional collaboration
Communication skills

Ausbildung

Bachelor’s degree or RN in related field

Tools

CTMS
EDC
eDiary
ePROs
TMF
IVRS/IWRS

Jobbeschreibung

Syneos Health, Inc. is seeking a Clinical Trial Manager II for Ciudad de Mexico with remote work options. You’ll oversee site management, monitoring, and data integrity across studies, coordinating with cross-functional teams.

The role emphasizes patient safety, regulatory compliance, and risk mitigation to ensure trial success. The incumbent will manage RA/monitoring activities, contribute to risk assessments, and drive timelines and budgets while supporting protocol execution and sponsor

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