Manager, Instrument Licensing, Pcs

IQVIA UK

São Paulo, Brazil
Manage assigned team of cpc/pma
Ensure project milestones are met
Compliance with sops and policies
Supervise and manage an assigned team of CPC/PMA and their subsidiaries, who manage or support project management activities to mitigate risk, control cost, project schedule and ensure quality, time and budget deliverables are completed to the Sponsor's satisfaction in accordance with applicable SOPs, policies and practices

Job Summary

  • Supervise and manage an assigned team of CPC/PMA and their subsidiaries, who manage or support project management activities to mitigate risk, control cost, project schedule and ensure quality, time and budget deliverables are completed to the Sponsor's satisfaction in accordance with applicable SOPs, policies and practices.
  • Ensure that employees are trained, and individual development is aligned and in place to meet project and organizational needs.
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Matching Summary

Supervise and manage an assigned team of CPC/PMA and their subsidiaries, who manage or support project management activities to mitigate risk, control cost, project schedule and ensure quality, time and budget deliverables are completed to the Sponsor's satisfaction in accordance with applicable SOPs, policies and practices.

Skills & Requirements

Must-have

  • Manage assigned team of CPC/PMA
  • Ensure project milestones are met
  • Compliance with SOPs and policies
  • Manage project schedule and budget
  • Train and onboard new hires
  • Review project performance dashboard
  • Resource allocation and utilization

Nice-to-have

  • Align individual development
  • Support EES action planning
  • Continuous improvement activities
  • Develop process improvements
  • High awareness of cultural differences

Key Requirements

  • Bachelor's degree in life sciences or related field
  • 5 years clinical research experience
  • 3 years leadership experience
  • Experience managing people
  • Knowledge of clinical trial conduct
  • Applicable clinical research regulatory requirements

Work Rights

Not specified

Tailored Resume

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