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Clinical Compliance Manager

ARTO

ARTO is partnered with an exciting, well-established global pharmaceutical company.

We are helping them source a Clinical Compliance Manager capable of acting as subject matter expert for all clinical quality matters whilst collaborating with cross functional internal & external teams in the clinical development programs to ensure quality throughout.

Clinical Compliance Manager

Responsibilities

  • Liaise between clinical functions and clinical development teams including quality assurance
  • Monitor and update policies and procedures (SOP) to include regulatory changes
  • Implement, Maintain, Develop and Evaluate quality assessments and performance improvement programs with cross functional teams
  • Overseeing compliance aspects of relevant third-party providers
  • Advise & support clinical development teams with GCP or Quality issues
  • Developing company compliance communications
  • Leading all key compliance projects including Business integrity, HCP transparency, data protection, anti-bribery and anti-corruption policies
  • Experience working with HCTP

Experience

The ideal candidate possesses:

  • Profound knowledge of ICH-GCP and proven track record of audit and inspection planning/preparation
  • Fluent spoken and written English
  • At least 5 years in the pharmaceutical industry within an international/global legal or compliance role
Upload your CV/resume or any other relevant file. Max. file size: 128 MB.