Senior Clinical Quality Manager – FSP Delivery Unit

IQVIA Inc; Madrid; On-site; EUR 90,000 - 120,000; Full time

Job summary

IQVIA is seeking an experienced Quality Management professional to define and drive the global Quality Plan across designated units. The role collaborates with global teams to ensure GCP compliance and continuous improvement in quality indicators.

The ideal candidate has extensive clinical trial design and regulatory knowledge, with a track record in CRO/pharma settings. Strong communication and stakeholder management are essential.

Qualifications

• Expert knowledge of and experience in clinical trial processes and regulatory environment.
• Knowledge of National and International Regulations and Drug Development processes.
• Experience in CRO or Pharmaceutical industry operations.
• Excellent problem solving skills.
• Ability to build effective relationships with stakeholders.
• Fluent in English.

Responsibilities

• Adopt and implement the global Quality Management Plan within the assignment scope.
• Identify and assess risks through data review and quality control processes.
• Support risk mitigation and corrective/preventive actions.
• Assist staff to improve compliance with ICH, GCP, SOPs and KPIs.
• Collaborate with stakeholders to maintain quality in project delivery.
• Develop and monitor a Delivery Unit/Sponsor quality management plan and risk program.
• Provide guidance on GCP compliance and quality issues.
• Inform Quality Management and lines of business about quality issues per SOPs.
• Assist during audits and regulatory inspections when required.
• Prepare periodic quality-related reports to business lines.

Skills

Fluent English

Problem solving

Quality mindset

Job description

IQVIA is seeking an experienced Quality Management professional to define and drive the global Quality Plan across designated units. The role collaborates with global teams to ensure GCP compliance and continuous improvement in quality indicators.

The ideal candidate has extensive clinical trial design and regulatory knowledge, with a track record in CRO/pharma settings. Strong communication and stakeholder management are essential.