Director, Global Medical Evaluation & Case Management

CSL Plasma; Wigan; On-site; GBP 60,000 - 85,000; Full time

Job summary

A global biotherapeutics company based in Wigan is seeking an experienced pharmacovigilance manager to oversee case processing within the global pharmacovigilance database. The role requires a minimum of 10 years of experience in Clinical Trials and Post-marketing Pharmacovigilance, with at least 5 years in a managerial capacity. Candidates should have a solid understanding of regulatory guidelines and successful track records in managing medicinal evaluations. This is an opportunity to contribute meaningfully to patient safety and therapeutic innovation.

Benefits

Comprehensive benefits

Inclusive workplace culture

Opportunities for career development

Qualifications

• Minimum of 10 years of Clinical Trial and Post-marketing Pharmacovigilance experience.
• 5 years of managerial/leadership experience is required.
• Proficient knowledge of global and local regulatory rules and regulations.

Responsibilities

• Oversee case management processes in pharmacovigilance.
• Ensure vendor compliance with regulatory guidelines.
• Lead departmental planning and resource allocation.

Skills

Clinical Trial experience

Post-marketing Pharmacovigilance experience

Managerial experience

Knowledge of global regulatory rules

Education

BS/BA, RN, Pharmacist, or similar

Job description

A global biotherapeutics company based in Wigan is seeking an experienced pharmacovigilance manager to oversee case processing within the global pharmacovigilance database. The role requires a minimum of 10 years of experience in Clinical Trials and Post-marketing Pharmacovigilance, with at least 5 years in a managerial capacity. Candidates should have a solid understanding of regulatory guidelines and successful track records in managing medicinal evaluations. This is an opportunity to contribute meaningfully to patient safety and therapeutic innovation.