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Sr Pharmacovigilance Specialist

1-2 years
€35,000 – €50,000 annually
10 May 23, 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

Job Title: Sr Pharmacovigilance Specialist
Location: Zaragoza, Spain
Category: Pharmacy & Clinical
Job Type: Full Time
Posted Date: March 26th, 2025
Job ID: R255953
Salary Estimate: €35,000 – €50,000 annually (based on local market and experience level)

About Cencora:
At Cencora, our team members are the cornerstone of everything we achieve. We are united by a mission to create healthier futures and improve lives—both human and animal. Join us and help shape the future of health with a company that values innovation, integrity, and purpose.

Position Summary:
Pharmalex, a part of Cencora, is seeking a skilled and driven Senior Pharmacovigilance (PV) Specialist to support one of our leading pharmaceutical partners. This remote position is based in Spain, and fluency in Portuguese, English, and Spanish is essential. The ideal candidate will bring 1–2 years of experience in Pharmacovigilance or Drug Safety and will be responsible for managing and supporting local PV operations and compliance.

Key Responsibilities:

  • Establish and oversee the local pharmacovigilance system in Spain.

  • Conduct Local Literature Search for safety information.

  • Manage Local ICSR (Individual Case Safety Reports) submissions.

  • Screen and analyze PV Intelligence updates.

  • Implement and monitor local Organized Data Collection systems.

  • Oversee and manage Local PVA (Pharmacovigilance Agreements).

  • Adapt and submit PSUR (Periodic Safety Update Reports) and RMPs (Risk Management Plans) locally.

  • Coordinate and implement additional Risk Minimization Measures.

  • Review local post-authorization safety-related materials.

  • Participate in audits and inspections related to PV compliance.

  • Generate monthly reports on local PV system status.

  • Ensure PV training for affiliates, third-party providers, and internal teams.

  • Collaborate with global PV teams and various local/global departments.

  • Review and maintain SOPs and Working Practices for local PV tasks.

  • Cooperate closely with designated Deputy, ensuring they are informed of all relevant activities.

  • Support and define PV-related processes in local clinical study protocols to ensure full compliance.

Requirements:

  • Minimum: College-level education; Degree in Life Sciences preferred.

  • 1–2 years of experience in Pharmacovigilance, Drug Safety, Clinical Research, or equivalent pharmaceutical roles.

  • Knowledge of global PV regulations (Health Canada, FDA, EMA, ICH guidelines).

  • Strong adaptability and willingness to learn.

  • Experience with medical/pharmaceutical terminology is an asset.

  • Fluent in Portuguese, English, and Spanish.

What Cencora Offers:
Our benefits go beyond standard offerings and are tailored to support wellness across physical, emotional, financial, and social dimensions. Depending on local market practices, benefits may include:

  • Comprehensive health coverage

  • Paid parental and caregiver leave

  • Training and professional development programs

  • Mentorship and employee resource groups

  • Volunteer opportunities and community engagement

Equal Opportunity Employer:
Cencora is an equal opportunity employer committed to fairness, inclusivity, and diversity in the workplace. We provide accommodations for individuals with disabilities during the recruitment process, in compliance with applicable laws.

Affiliated Company: Pharmalex