Clinical Project Manager - Iqvia Biotech - Oncology

IQVIA Inc

5 years relevant experience
1 year project management experience
Knowledge of ich gcp regulations
Project Leads are responsible for the execution of clinical studies to meet contractual requirements while optimizing speed, quality, and cost

Job Summary

  • Project Leads are responsible for the execution of clinical studies to meet contractual requirements while optimizing speed, quality, and cost.
  • The role involves developing integrated study management plans and setting objectives for core project teams to ensure milestone achievement.
  • Candidates must possess advanced knowledge of clinical trial conduct and apply regulatory requirements such as ICH GCP effectively.

Matching Summary

Project Leads are responsible for the execution of clinical studies to meet contractual requirements while optimizing speed, quality, and cost.

Skills & Requirements

Must-have

  • 5 years relevant experience
  • 1 year project management experience
  • Knowledge of ICH GCP regulations
  • Clinical trial conduct expertise
  • Cross-functional team leadership

Nice-to-have

  • Therapeutic expertise in oncology
  • Bid defense presentation skills
  • Vendor management capabilities
  • Strategic leadership abilities
  • Mentoring less experienced staff

Key Requirements

  • Bachelor's Degree in Life Sciences
  • Minimum 5 years prior relevant experience
  • Minimum 1 year project management experience
  • Advanced knowledge of clinical research regulatory requirements

Work Rights

Not specified

Tailored Resume

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