Global Program Safety Lead - CRM
Novartis · Barcelona Gran Vía · Global
Regulatory Affairs
–
Not yet analysed
Demand80
Career growth85
Healthcare fit85
Remote potential70
5-year outlook
Competitive executive-level compensation with bonuses; typically in the top percentile for pharmaceutical roles, though exact figures depend on experience and location.
Clinical license
Required
Applicant reach
narrow
Seniority
senior
Employment type
–
Date found
2026-09-14
Intelligence details
Why this is worth applying to
If you have pharmacovigilance or drug safety experience, this is a strong opportunity. Without that background, it may be a stretch, but clinical expertise is highly valued.
Who should apply
Physicians with clinical trial or drug safety experience, especially in cardiovascular, renal, or metabolic areas.
CV angle
Highlight clinical expertise, understanding of adverse events, regulatory knowledge, and any prior pharmacovigilance or drug development experience.
Skills to highlight
- Pharmacovigilance
- Regulatory affairs
- Clinical development
- Risk management
- Leadership
- Signal detection
- Safety data analysis
Role summary
Global lead for safety of a drug program in the CRM (cardiovascular, renal, metabolic) therapeutic area, overseeing pharmacovigilance activities and regulatory compliance.
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