Pharmacovigilance Scientist (Hybrid)

4-5 years

Not Disclosed

Madrid

10 Jan. 3, 2025

Job Description

Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Scientist (Hybrid)
Location: Madrid, Spain
Date Posted: January 3, 2025

Join Teva Pharmaceuticals, a global leader in pharmaceuticals, dedicated to improving health and delivering accessible, high-quality medicines to millions worldwide.

Role Overview

As a Pharmacovigilance Scientist, you will ensure compliance with local and international pharmacovigilance regulations, support drug safety processes, and contribute to the seamless integration of safety protocols within Teva’s operations.

Key Responsibilities:

Regulatory Compliance: Stay updated on local pharmacovigilance legislation and ensure adherence to Teva's global practices, policies, and procedures.
Process Oversight: Manage corrective and preventive actions (CAPA) related to pharmacovigilance deviations and draft internal procedures when necessary.
Risk Management: Monitor and implement risk minimization plans (RMPs) and additional risk minimization measures (aRMM) as agreed with national authorities.
Adverse Event Management: Handle adverse drug reactions, special event reports, and safety issues for medical devices, cosmetics, and other non-medicinal products.
Literature Monitoring: Conduct local literature surveillance to identify potential safety concerns or cases.
Training: Develop and deliver pharmacovigilance training for Teva Spain employees, tailored to individual roles and responsibilities.
Documentation and Reporting: Translate pharmacovigilance documentation between Spanish and English, reconcile data internally and externally, and prepare reports.
Collaboration: Ensure compliance with safety information-sharing agreements between Teva and third parties, working seamlessly across local, European, and international teams.

Qualifications:

Education:
- Bachelor’s or Doctorate in life sciences, pharmacy, or medicine.
- Master’s in pharmaceutical industry (preferred).
Experience:
- 4-5 years of proven experience in healthcare or pharmaceutical industry/pharmacovigilance.
Skills:
- Fluent in Spanish and English (written and spoken); Portuguese is a plus.
- Strong communication and interpersonal abilities.
- Proficient in industry-standard IT tools.
- Capable of managing multiple tasks, prioritizing workloads, and solving complex problems with creativity.
Other Competencies:
- Customer-focused mindset.
- Proactive and responsible attitude with strong organizational skills.
- Team-oriented and skilled in fostering collaborative relationships.

Reporting To:
Pierre-Antoine Sauton (Associate Director, Local Safety Officer, Head of Pharmacovigilance Spain)

Why Join Teva?

Work with a company treating over 200 million patients daily.
Be part of a mission-driven organization committed to health, sustainability, and innovation.
Enjoy a collaborative and inclusive workplace with opportunities for growth.

Application for Current Teva Employees:
Apply through the Internal Career Site on "Employee Central" for priority consideration and access to exclusive opportunities.

Equal Opportunity Commitment:
Teva Pharmaceuticals upholds equality in employment, offering opportunities regardless of age, race, gender, disability, or any other legally protected status. Accommodations are provided to ensure a fair recruitment process.

For more information, visit the Teva Careers page and take the next step in making a global impact.

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Pharmacovigilance Scientist (Hybrid)

Job Description

Role Overview

Key Responsibilities:

Qualifications:

Why Join Teva?

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