Senior Manager, QPPV Office

Job not on LinkedIn

🔥 44 minutes ago

🌐 Bulgaria, Portugal, +2 more countries – Remote

🇧🇬 Bulgaria – Remote 🇵🇹 Portugal – Remote 🇮🇳 India – Remote 🇪🇸 Spain – Remote

⏰ Full Time

🟠 Senior

👔 Manager

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Cencora

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

📦 Logistics

🏥 Healthcare

Consulting • Logistics • Healthcare

Cencora is a company dedicated to improving the health and well-being of both people and animals globally. Built on the legacy of AmerisourceBergen, Cencora offers a wide range of industry-leading solutions that encompass specialty logistics, warehousing, drug research, clinical development support, and more. They provide commercialization and patient access support and offer wholesale and specialty distribution services. Cencora serves a diverse clientele, including pharmaceutical companies, physician practices, pharmacies, and health systems. The company also extends its services to animal health, managing operations and delivering products for animal pharmaceutical care. With a strong global footprint, Cencora aims to reshape healthcare delivery through innovative products and solutions, striving to create healthier futures for all.

📋 Description

• Own the pharmacovigilance agreement (PVA) management process • Oversee and coordinate the timely preparation of authority-relevant documents • Conceptualize and develop templates, project-specific documents, and processes

🎯 Requirements

• At least two years of experience in global pharmacovigilance (not case processing), including specifically PVA management • 4+ years of experience in pharmacovigilance, drug safety, epidemiology, risk management, scientific consulting, regulatory affairs, or a related field • Bachelor's degree in life sciences, pharmacy, medicine, nursing, public health, epidemiology, regulatory affairs, or a related field, or equivalent experience required • Certification in pharmacovigilance or drug safety preferred • Certification in regulatory affairs, clinical safety preferred • Certification in quality management or auditing preferred

🏖️ Benefits

• Benefit offerings outside the US may vary by country and will be aligned to local market practice • Reasonable accommodations during the employment process for individuals with disabilities