Global Good Clinical Practices / Pharmacovigilance Auditor
Novartis · 2 Locations · Global
Posted 60+ days ago
Regulatory Affairs
–
Not yet analysed
Demand80
Career growth75
Healthcare fit85
Remote potential60
5-year outlook
Competitive for pharma compliance roles, typically six-figure salaries with experience; growth tied to regulatory complexity and global drug safety demands.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
–
Date found
2026-09-04
Intelligence details
Why this is worth applying to
Yes for clinicians with clinical research or pharmacovigilance experience; the role leverages clinical knowledge in a high-impact compliance setting. Without relevant experience, it may be a stretch.
Who should apply
Doctors, pharmacists, and nurses with clinical trial or drug safety experience, especially those interested in regulatory affairs and quality assurance.
CV angle
Highlight clinical trial participation, understanding of GCP, patient safety awareness, attention to detail, and any experience with audits or regulatory inspections.
Skills to highlight
- Good Clinical Practices (GCP)
- Pharmacovigilance
- Regulatory Compliance
- Clinical Research
- Auditing
- Data Integrity
- Risk Assessment
Role summary
Audits global clinical trials and pharmacovigilance systems to ensure compliance with regulatory standards and patient safety requirements.
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