Global Clinical Quality & Compliance Leader

C50 Cochlear Benelux NV (Belgium); Antwerpen; Sur place; EUR 85 000 - 115 000; Plein temps

Avantages offerts par ce poste

Attractive remuneration package

Flexible extra-legal benefits

Extensive onboarding and training

Résumé du poste

Cochlear Benelux NV (Belgium) is seeking a Clinical Quality and Compliance (CQC) Manager to strengthen quality, compliance and systems supporting global clinical research activities. You will provide GCP and ISO 14155 expertise, drive improvements, support audits and maintain robust QMS processes across sites, vendors and stakeholders.

The role combines hands-on regulatory work with system and process ownership, requiring collaboration across regions and time zones, with occasional travel and a

Qualifications

• Bachelor's degree in Healthcare, Life Sciences, Nursing, Public Health or equivalent.
• Strong knowledge of GCP and clinical research regulations is preferred.
• Excellent attention to detail with strong organisational and communication skills.

Responsabilités

• Support CQC quality management activities and QMS change management.
• Provide SME on GCP, ISO 14155 and applicable local clinical investigation regulations.
• Support the assessment and implementation of new or revised clinical research standards.
• Contribute to clinical investigation quality oversight and audit readiness.
• Assist with quality assurance through risk/issue management, inspections, and reporting.
• Act as Clinical Business and System Administrator for Vault Clinical; support UAT, training and licensing/budget tasks.
• Collaborate with regional stakeholders on privacy, outsourcing and contracts.

Connaissances

English fluency

Attention to detail

Organisational skills

Time management

Communication skills

Formation

Bachelor's degree in Healthcare, Life Sciences, Nursing, Public Health or equivalent

Description du poste

Cochlear Benelux NV (Belgium) is seeking a Clinical Quality and Compliance (CQC) Manager to strengthen quality, compliance and systems supporting global clinical research activities. You will provide GCP and ISO 14155 expertise, drive improvements, support audits and maintain robust QMS processes across sites, vendors and stakeholders.

The role combines hands-on regulatory work with system and process ownership, requiring collaboration across regions and time zones, with occasional travel and a