Principal Manager, Clinical Quality Management

ICON Clinical Research, LP

8-10 years biopharmaceutical industry experience
Sponsor/cro gcp experience required
Strong operational understanding of clinical trials
The role involves leading document development, revision, and retirement processes aligned with sponsor procedures and quality standards

Job Summary

  • The role involves leading document development, revision, and retirement processes aligned with sponsor procedures and quality standards.
  • Candidates must support internal and external audits by providing documentation and ensuring timely resolution of findings.
  • ICON offers competitive benefits including health insurance, retirement planning, and a global Employee Assistance Programme.

Matching Summary

The role involves leading document development, revision, and retirement processes aligned with sponsor procedures and quality standards.

Skills & Requirements

Must-have

  • 8-10 years biopharmaceutical industry experience
  • Sponsor/CRO GCP experience required
  • Strong operational understanding of Clinical Trials
  • Process/Controlled Document Management knowledge
  • Exemplary organization and communication skills

Nice-to-have

  • Experience in a Clinical Project Manager role
  • Ability to facilitate conversations with SMEs
  • Interest in improving Global Clinical Operations
  • Exemplary QC skills

Key Requirements

  • Bachelor's degree in life sciences preferred
  • 8-10 years of experience in biopharmaceutical industry
  • Sponsor/CRO GCP experience required

Work Rights

Not specified

Tailored Resume

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