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Den här rollen kommer från Arbetsförmedlingen. Vi visar den här först på Marketplace så att kandidaten kan läsa vidare, jämföra liknande roller och fortsätta till ansökan när det passar.
Rollöversikt
Matchad från extern källa med fokus på medical contact center assistant i - swedish speaker i Karlstad · Värmlands län · Sverige. Nästa steg är att öppna ansökan hos Arbetsförmedlingeneller fortsätta jämföra liknande jobb direkt här på Marketplace.
Villkor och krav
Anställningsform: Vanlig anställningArbetstid: HeltidOmfattning: 100-100%Lön: Lön enligt överenskommelseLönetyp: Fast månads- vecko- eller timlönSista ansökan: 5 september 2026Erfarenhet: Krävs
Ansökan och signaler
Full rollbeskrivning
Your Role at Fortrea: As a Medical Contact Center Assistant I, you will be the voice of support for healthcare professionals and patients, addressing medical information queries, product quality complaints, and general inquiries. You will also be responsible for receiving, recording, and reporting Adverse Drug Reactions (ADRs) in compliance with regulatory timelines and internal SOPs. What You Will Be Doing:
- Handle incoming communications via phone, email, fax, etc., providing accurate responses to inquiries.
- Record and report adverse events efficiently and in accordance with regulatory and internal standards.
- Support activities such as data tracking, quality control, training support, and data reconciliation.
- Collaborate across departments and maintain high standards of documentation and communication.
- Perform other assigned duties as needed.
- Fluency in Swedish (C1 or higher) is mandatory.
- A degree in Pharmacy, Life Sciences, MD, VET or related fields is preferred, but equivalent experience is considered.
- Pharmacovigilance or Drug Safety
- Clinical Data Entry/Management
- Medical Affairs or Regulatory Affairs
- Quality Assurance in the pharmaceutical/biotech/CRO industry
- Processing AE/SAE reports
- Narrative generation
- Query management
- Using safety databases
- Regulatory submissions
- Clear written and verbal communication
- Good grasp of regulatory guidelines (ICH GCP, Pharmacovigilance standards)
- High attention to detail and accuracy
- Proficiency with Microsoft Office
- Team player who can also work independently with moderate supervision