Senior GCP Compliance Director - Hybrid (Barcelona)

Novartis

Sabadell

Hybrid

EUR 85,000 - 158,000

Full time

34 hours ago
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Job summary

Novartis in Barcelona is seeking a senior GCP Compliance leader to oversee Global Clinical Operations and drive QA excellence in a hybrid work setup. You will mentor a team across trials, ensure regulatory alignment, and partner with cross-functional leaders to elevate portfolio quality.

Ideal candidates hold an advanced Life Sciences degree, 10+ years in clinical research, and a proven track record in audits, inspections, and CAPA leadership.

Qualifications

  • Advanced degree in Life Sciences or related discipline.
  • 10+ years in clinical research/pharma.
  • Proven leadership in global matrix organizations.
  • GCP, regulatory standards, and QA knowledge.

Responsibilities

  • Provide compliance oversight of regulated Global Clinical Operations activities across assigned Development Units and clinical trial portfolios.
  • Lead, coach, mentor, and develop a high-performing team of GCP Compliance Managers.
  • Drive compliance oversight of programs and trials ensuring GCP and regulatory alignment.
  • Oversee QA delivery, including audits, inspections, quality issues, and CAPA activities.
  • Lead audit/inspection readiness, including response management and corrective actions.
  • Identify quality trends and communicate risks to leadership.
  • Collaborate with DU leadership, QA, and cross-functional stakeholders to improve portfolio quality.

Skills

Leadership
GCP knowledge
Regulatory knowledge
Audits & inspections
Strategic thinking
Cross-functional collaboration

Education

Advanced degree in Life Sciences

Job description

Novartis in Barcelona is seeking a senior GCP Compliance leader to oversee Global Clinical Operations and drive QA excellence in a hybrid work setup. You will mentor a team across trials, ensure regulatory alignment, and partner with cross-functional leaders to elevate portfolio quality.

Ideal candidates hold an advanced Life Sciences degree, 10+ years in clinical research, and a proven track record in audits, inspections, and CAPA leadership.

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