Manager, Quality Assurance
ICON · Ankara, Turkey +1 more
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Role summary
This role involves overseeing quality assurance and compliance activities for clinical trials, including developing QA strategies, conducting audits, and ensuring regulatory adherence. The successful candidate will manage quality issues, support team development, and collaborate across project teams. Requires a bachelor's degree, minimum 5 years of QA experience in pharmaceuticals or CROs, and knowledge of clinical trial regulations.
What they're looking for
- Bachelor's degree in relevant discipline
- Minimum 5 years quality assurance experience in pharmaceutical, biotechnology, or CRO
- Knowledge of ICH-GCP and FDA regulatory requirements for clinical trials
- Strong analytical and problem-solving abilities for quality issue resolution
- Excellent cross-functional communication and stakeholder collaboration skills
- Willingness to travel approximately 35% as required
What you'll be doing
- Develop and implement quality assurance strategies and processes for clinical trials
- Conduct quality assessments and audits to ensure regulatory compliance
- Collaborate with project teams to identify and resolve quality issues
- Provide guidance to staff on quality policies, procedures, and best practices
- Contribute to quality management systems and documentation development
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.