Global Clinical Quality Manager (FSP)

IQVIA; Reading; On-site; GBP 65,000 - 90,000; Full time

Job summary

IQVIA is a leading global provider of clinical research services with a strong focus on quality management and regulatory compliance. This role supports the global Quality Management team, ensuring adherence to GCP, SOPs, and KPIs across designated units and tasks.

The position emphasizes risk assessment, corrective actions, and collaboration with sponsors, business lines, and stakeholders to drive compliant and efficient delivery in a complex regulatory landscape.

Qualifications

• Expert knowledge of and experience in clinical trial design, planning, start up, conduct, analysis, and reporting (8+ years).
• Knowledge of National and International Regulations and Drug Development processes.
• Knowledge of CRO or Pharmaceutical industry operations.
• Excellent problem solving skills.
• Ability to establish and maintain effective working relationships.

Responsibilities

• Adopt and implement the global Quality Management Plan across units and tasks.
• Support risk identification, assessment, and mitigation.
• Collaborate with stakeholders to ensure quality in project delivery.
• Provide advice on GCP compliance and SOP adherence.
• Manage non-compliance and coordinate corrective/preventive actions.
• Inform Quality Management and stakeholders of quality issues per SOPs.
• Support audits and regulatory inspections as needed.
• Act as primary QA contact and attend meetings.
• Prepare periodic quality reports for business lines.
• Perform other tasks as required by the LM.

Skills

Quality management

GCP compliance

Risk management

English fluency

Job description

IQVIA is a leading global provider of clinical research services with a strong focus on quality management and regulatory compliance. This role supports the global Quality Management team, ensuring adherence to GCP, SOPs, and KPIs across designated units and tasks.

The position emphasizes risk assessment, corrective actions, and collaboration with sponsors, business lines, and stakeholders to drive compliant and efficient delivery in a complex regulatory landscape.