Senior Specialist, Client Facing Scientific Consulting

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🌐 Spain, Bulgaria – Remote

🇪🇸 Spain – Remote 🇧🇬 Bulgaria – Remote

⏰ Full Time

🟠 Senior

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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

• Prepare and maintain project-related documents • Compile PSMFs, act as PSMF Coordinator, and ensure review/approval by the QPPV and timely submission to authorities as needed • Quality check PSMFs prior to QPPV approval • Work on pharmacovigilance projects for clients based on experience and qualification • Negotiate, update, and terminate PVAs, including SDEAs, PV Service Agreements, and Quality Technical Agreements • Perform administrative tasks supporting the QPPV and the PER PV GOV Practice Area • Act as Project Lead for small projects such as QPPV/PSMF or PVA services • Take over primary tasks and responsibilities in other service lines, project management activities as client contact point, and additional reasonable tasks aligned with abilities, qualification, and training

🎯 Requirements

• University degree in Life Sciences preferred but not essential • Experience in pharmacovigilance, drug safety, epidemiology, risk management, scientific consulting, regulatory affairs, or a related field required • Certification in pharmacovigilance or drug safety preferred • Certification in regulatory affairs or clinical safety preferred • Certification in quality management or auditing preferred • Ability to perform responsibilities aligned with abilities, qualification, and training

🏖️ Benefits

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