Associate Country Clinical Quality Manager

As a (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

• This role is responsible for support and performance of clinical trials quality activities that mainly fall under the scope of ICH-GCP (Good Clinical Practice). CCQM is expected to be the local expert for ICH-GCP and local regulations related to clinical trials. The role supports a large team of local clinical operations team in Turkey and acts as a quality bridge between local team and Regions & Head Quarters.
• CCQM role is responsible for the oversight and/ or execution of the activities indicated in clinical quality management system (cQMS) of Audit and Inspection Support, Training Support, Consultation, Process Implementation and Management, Quality Control, Supplier Qualification and Oversight, Quality Issue Management.
• The role reports to CCQM Lead in Turkiye.

• Minimum 5 years of relevant experience in clinical research including direct field monitoring experience or management/oversight of such individuals, with a demonstrated record of accomplishments.
• Deep knowledge and understanding of Clinical Trial processes as well as quality management and control tools is required. 
• Demonstrated experience leading cross-functional teams of business professionals.
• Solid track record of initiating, planning and delivery of projects and knowledge of project management practices.
• Candidates with experience in quality management / compliance (e.g. audit/inspection support incl. CAPA management, SOP management, compliance issue management) will be preferred.

Why ICON?

Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.