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
If you’d like to learn more about this opportunity please reach out and I’ll be happy to have a confidential discussion in more detail over a call.
