Medical Information Specialist

Job not on LinkedIn

🔥 21 hours ago

🇪🇸 Spain – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

👻 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

• Address Medical Information requests (MIR) from multiple programs and sources using approved response documents • Ensure all MIR are processed and documented according to organization and client procedures and project working practice • Identify and document adverse events (AE), product complaints, and quality issues • Report adverse event information to the pharmacovigilance department • Collaborate with internal teams, including regulatory, medical affairs and marketing, to provide scientific support • Participate in client product training, diseases and therapeutic areas, as required by the project • Support the project team with report clarification, metrics, volumes, KPIs and compliance investigations • Escalate L2 MIR according to project agreement • Support internal and external audits • Perform quality control of MIR to ensure adherence to project requirements and procedures • Reconcile medical information reports with adverse events and product quality complaint reports within agreed timelines

🎯 Requirements

• Bachelor's degree in life sciences, pharmacy, biomedical sciences, public health, or a related field, or equivalent experience required • Less than 2 years of experience in scientific consulting, healthcare, life sciences, or a related field required • Required proficiency in Spanish, English and German language • Certification in clinical research or regulatory affairs preferred • Certification in data analytics or scientific data interpretation tools preferred

🏖️ Benefits

• Benefit offerings outside the US may vary by country and will be aligned to local market practice • Equal employment opportunity and non-discriminatory recruiting, training, compensation, benefits, promotions and transfers • Reasonable accommodations during the employment process