Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Pv Specialist- Clinical Safety

1+ years
Not Disclosed
10 May 22, 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: PV Specialist – Clinical Safety
Category: Pharmacy & Clinical
Location: Madrid, Spain
Job Type: Full Time
Posted Date: March 13, 2025
Job ID: R255103


About Cencora:

At Cencora, our people drive our mission to create healthier futures. We are united by a shared commitment to make a positive impact in healthcare. Join our innovative and fast-growing team to contribute meaningfully to improving the lives of people and animals worldwide.


Job Description:

We are seeking a Pharmacovigilance (PV) Specialist – Clinical Safety to support the growing Clinical Safety function within the PharmaLex brand. This remote-based position in Spain offers an excellent opportunity for professionals looking to expand their expertise in safety surveillance and case management activities.


Key Responsibilities:

  • Oversee the full lifecycle of SAEs, AESIs, and pregnancy cases, including case tracking and follow-ups

  • Ensure timely communication with involved stakeholders and follow up on pending information

  • Conduct initial triage for seriousness and expectedness of reported events

  • Perform data entry in safety databases and write narratives

  • Assist Safety Manager with quality control (QC) reviews in the safety database

  • Prepare Line Listings (LLs) and maintain annual plans and distribution lists for LLs and DSURs

  • Execute safety submissions and manage administrative trackers and documents


Required Skills:

  • Strong team collaboration and interpersonal skills

  • Excellent organizational ability and capability to multitask

  • Ability to analyze and interpret data quickly

  • Self-driven with a high sense of responsibility

  • Adaptable and flexible in facing new and dynamic challenges

  • Fluent in spoken and written English

  • Strong communication skills, both verbal and written


Qualifications & Experience:

  • Bachelor’s degree in medicine, natural sciences, or pharmacy-related field (Degree in Medicine also accepted)

  • Minimum 1 year of professional experience in Pharmacovigilance

  • Hands-on experience with safety databases (Argus, Safety Easy preferred)

  • Prior experience in case management and in the pre-authorization phase


What Cencora Offers:

  • Benefits tailored to local market standards (eligibility and availability may vary)

  • A diverse and inclusive workplace

  • Commitment to Equal Employment Opportunity and non-discriminatory practices

  • Reasonable accommodations available upon request for individuals with disabilities


Affiliated Companies: PharmaLex Spain S.L.U.
📧 For accommodations:
hrsc@cencora.com
📞 Or call: 888.692.2272
🖥️ Visit:
www.cencora.com