Global Clinical Quality Leader - FSP

IQVIA Inc; Warszawa; On-site; PLN 151,000 - 374,000; Full time

Job summary

IQVIA Inc in Poland is seeking a seasoned Quality Management professional to join our Delivery Unit and sponsor teams in Warsaw. You will define and adopt the global Quality Plan, ensure GCP compliance and risk management, and guide corrective/preventive actions to improve staff performance and processes.

You will collaborate with global/ regional Quality Management and other stakeholders to monitor KPIs, implement SOPs, and advise on quality control across clinical staff and projects.

Qualifications

• Bachelor's degree or equivalent qualification is required.
• At least 7 years of overall working experience.
• At least 3 years of extensive GCP experience.
• Knowledge of regulatory and drug development processes.
• Experience in CRO or pharmaceutical operations.
• Strong organizational and communication skills.
• Ability to travel within the region/country.
• Ability to lead and motivate a clinical team.
• Strong stakeholder management and interpersonal skills.

Responsibilities

• Adopt and implement the global Quality Management Plan within the assignment scope.
• Identify risks and support corrective/preventive actions.
• Collaborate with stakeholders to maintain quality focus in projects.
• Develop and monitor a Delivery Unit/ Sponsor quality plan and risk program.
• Provide guidance on GCP compliance and quality issues.
• Assist audits and regulatory inspections as agreed.
• Serve as primary Quality Assurance contact for quality matters.
• Prepare periodic quality reports for business lines.

Skills

Fluent in English

Education

Bachelor's Degree or equivalent qualification

Job description

IQVIA Inc in Poland is seeking a seasoned Quality Management professional to join our Delivery Unit and sponsor teams in Warsaw. You will define and adopt the global Quality Plan, ensure GCP compliance and risk management, and guide corrective/preventive actions to improve staff performance and processes.

You will collaborate with global/ regional Quality Management and other stakeholders to monitor KPIs, implement SOPs, and advise on quality control across clinical staff and projects.