Added
19 days ago
Type
Full time
Salary
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Related skills

gcp clinical trials ich ms project microsoft excel

📋 Description

  • Support development and maintenance of project plans, timelines, milestones, deliverables, and
  • Coordinate biometrics activities across Biostatistics, Statistical Programming, and Data Management.
  • Track study progress against contracted scope, timelines, and key milestones.
  • Follow up with functional leads and team members regarding deliverables, dependencies, and
  • Support database lock, analysis, reporting, and other critical biometrics milestones.
  • Assist with planning and coordination of multiple studies or workstreams.

🎯 Requirements

  • Requires a bachelor’s degree or higher in life sciences. MBA or PMP is preferred.
  • 0-2 years of relevant experience in Pharma/CRO industry. Basic understanding of the clinical
  • Previous experience in project coordination, clinical operations, Data Management, Biostatistics
  • Familiarity with project management concepts such as scope, timeline, budget, risk, dependencies
  • Knowledge of FDA regulations, drug development and PM processes.
  • Good understanding of ICH/GCP guidelines.
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