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Medical Information Specialist With Spanish And English Language

0-2 years
Not Disclosed
10 July 16, 2025
Job Description
Job Type: Remote 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

 

Medical Information Specialist (Spanish & English) – Oeiras, Portugal

Job Summary:
IQVIA is hiring a Medical Information Specialist fluent in Spanish and English for its Safety Operations team in Oeiras, Portugal. This key role supports global drug safety through medical inquiry handling, pharmacovigilance reporting, and product quality tracking. With direct communication to healthcare professionals and patients, you’ll help optimize the safety profiles of treatments across therapeutic areas such as Respiratory, Infectious Diseases, Immunology, Inflammation, HIV, and Oncology. Ideal for life science graduates seeking a patient-focused, multilingual career in healthcare.


Responsibilities:

  • Provide phone-based support for healthcare professionals and patients regarding medical inquiries, adverse events, and product quality issues.

  • Log and manage communications via calls, emails, and faxes from global sources during standard business hours.

  • Track and document safety data to meet pharmacovigilance compliance standards.

  • Communicate updates and challenges to project leads and local management teams.

  • Collaborate with the global Lifecycle Safety team to support continuous quality improvements.

  • Participate in training, cross-functional working groups, and implementation of process efficiencies.


Required Skills & Qualifications:

  • Bachelor’s Degree in Life Sciences or a healthcare-related discipline (mandatory).

  • Fluency in Spanish and English (minimum C1 level in both).

  • Strong attention to detail with a focus on accuracy and quality documentation.

  • Excellent organizational, time management, and multitasking capabilities.

  • Ability to build positive working relationships with internal teams and clients.

  • Willingness to learn new skills within IQVIA’s Lifecycle Safety operations.


Perks & Benefits:

  • Join the world’s largest drug safety department with extensive internal learning and career advancement opportunities.

  • Work on meaningful projects that impact global public health.

  • Collaborative and diverse work environment with a culture of inclusion.

  • Structured career ladder with support from experienced leadership.

  • Exposure to top pharmaceutical clients and varied therapeutic areas.


Company Overview:

IQVIA is a global leader in healthcare analytics, clinical research, and technology-driven life sciences services. The company partners with leading pharmaceutical and biotechnology companies to advance medical innovation, improve drug safety, and transform global health outcomes.


Work Mode: On-site – Oeiras, Portugal
Salary: Competitive (exact range not disclosed)


Ready to Make an Impact?

Start your career in global pharmacovigilance with IQVIA. Apply today to support patient safety and advance healthcare innovation worldwide.