Principal Manager, Clinical Quality Management

ICON

Not specified; competitive within each country; va...
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 possess strong operational understanding of Clinical Trials and GCP to manage project objectives and drive collaborative reviews.
  • ICON offers a competitive salary, diverse benefits including health insurance and retirement planning, and a culture focused on inclusion and well-being.

Matching Summary

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

Salary

Not specified; Competitive within each country; Various annual leave entitlements; Health insurance offerings; Retirement planning offerings

Skills & Requirements

Must-have

  • 8-10 years biopharmaceutical industry experience
  • Sponsor/CRO GCP experience required
  • Strong operational understanding of Clinical Trials
  • Project Management experience in clinical trials
  • Process/Controlled Document Management knowledge

Nice-to-have

  • Experience in a Clinical Project Manager role
  • Exemplary organization and communication skills
  • Facilitation skills for Subject Matter Experts
  • Exemplary QC skills
  • Interest in improving Global Clinical Operations

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter