Senior Clinical Quality Manager FSP Lead

IQVIA; Basel; On-site; CHF 150,000 - 210,000; Full time

Job summary

IQVIA Basel seeks an experienced Quality Management professional to implement and oversee the global Quality Plan across Delivery Unit(s) and sponsor activities, ensuring GCP compliance and risk management.

This senior individual contributor role emphasizes collaboration with global/regional teams, audits support, and reporting, requiring at least 8 years in clinical trial processes and fluent English.

Qualifications

• Minimum of 8 years of experience in clinical trial design, planning, start up, conduct, analysis, and reporting.
• Knowledge of National and International Regulations and Drug Development processes.
• Experience with CROs or pharmaceutical industry operations.
• Excellent problem solving skills.
• Ability to establish and maintain effective working relationships with co-workers, managers and clients/customers.
• Fluent in English.

Responsibilities

• Adopt and implement the global Quality Management Plan within the scope of the assignment; plan and execute Quality Management activities.
• Cooperate with relevant business and stakeholders to maintain focus on quality in project delivery.
• Develop and implement a Delivery Unit/Sponsor specific Quality Management plan and Risk Management Program; monitor implementation.
• Provide advice on GCP compliance to teams and stakeholders.
• Manage non-compliance and quality issues; plan corrective/preventive actions as per SOPs.
• Inform Quality Management, the assigned business line, and Quality Assurance of quality issues.

Skills

Clinical trial design

Quality management

Regulatory knowledge

Problem solving

Stakeholder management

English fluency

Job description

IQVIA Basel seeks an experienced Quality Management professional to implement and oversee the global Quality Plan across Delivery Unit(s) and sponsor activities, ensuring GCP compliance and risk management.

This senior individual contributor role emphasizes collaboration with global/regional teams, audits support, and reporting, requiring at least 8 years in clinical trial processes and fluent English.