*summary*:
at novartis, patient safety sits at the core of our purpose, and this role gives you the opportunity to make a real difference every day.
- as a patient safety specialist, you’ll help protect patients by ensuring safety information is collected, assessed, and reported with the highest standards of quality and compliance. Working closely with medical, regulatory, and operational partners, you’ll support country-level pharmacovigilance activities, contribute to inspections and audits, and strengthen a culture of collaboration, integrity, and continuous improvement.
*about the role*:
*job title*: patient safety specialist
*contract duration*: 12 months
*location*: insurgentes, mexico city, mexico
li-hybrid
*key responsibilities*
- collect, assess, document, and follow up safety reports from all sources, including clinical and post-marketing
- process adverse event cases in safety systems with accuracy, completeness, quality focus, and timeliness
- coordinate safety report submissions and safety information distribution to health authorities and partners
- collaborate with external service providers to ensure regulatory and procedural compliance
- develop, update, and implement local pharmacovigilance procedures aligned with global standards
- partner with cross-functional teams to ensure safety data capture and vigilance compliance
- provide guidance on vigilance clauses for local contracts and agreements
- track pharmacovigilance agreements and escalate deviations from standard templates
- reconcile safety data with medical, quality, and third-party partners
- support training, audits, inspections, and corrective and preventive action plans
*essential requirements*
- completed degree (or currently pursuing with expected graduation within the next 3 months) in a life sciences or healthcare discipline (e.g., pharmacy, chemistry, nursing, medicine, or equivalent).
- knowledge of national and international pharmacovigilance regulations
- experience in adverse event processing and safety reporting
- understanding of pharmacological and medical terminology
- strong attention to quality, accuracy, and regulatory timelines
- intermediate english (both spoken & written)
- fluency in local language (both spoken & written)
- strong communication and collaboration skills
*desirable skills*
- 1 year of experience in a similar role
*benefits and rewards*: learn about all the ways we’ll help you thrive personally and professionally.
- read our handbook (pdf 30 mb)
division
development
business unit
development
location
mexico
site
insurgentes
company / legal entity
mx06 (fcrs = mx006) novartis farmacéutica s.a. de c.v.
Functional area
research & development
job type
full time
employment type
regular
shift work
no
novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
*accessibility and accommodation*: