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ProPharma

Swedish Speaking Medical Information Specialist – 12 Month Contract

ProPharma

Medical Information Specialist answering Swedish and English safety enquiries for ProPharma, which supports pharmaceutical, biotech, and medical device companies. Documenting adverse events and delivering compliant medical responses remotely across the UK, Serbia, or Croatia.

Posted 8/4/2026full-timeRemote • 🇬🇧 United KingdomMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in responding to medical and safety-related inquiries while ensuring compliance with regulatory standards. Proficient in documenting adverse events and providing high-quality medical responses, with strong communication skills in both Swedish and English.

Highest-signal resume keywords
Degree In Life SciencesDrug SafetyMedical InformationRegulatory AffairsC1 Fluency In Swedish And English

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Documenting Adverse EventsProviding Medical ResponsesPerforming Safety ChecksUsing Scientific LiteratureLogging Enquiries
Soft Skills
Strong Written CommunicationStrong Verbal CommunicationAttention To DetailProactive MindsetWillingness To Learn
Tools & Technologies
Internal SystemsWeb Platforms
Industry Keywords
HealthcareSafety ConcernsProcess ImprovementsMentorshipAfter-Hours Coverage

About the role

Key responsibilities & impact
  • Respond to medical and safety-related enquiries from healthcare professionals, patients, and consumers via phone, email, and web platforms
  • Use approved product information, scientific literature, and internal data to provide clear, accurate responses
  • Document and report adverse events, product complaints, and other safety concerns in line with regulatory standards
  • Log all enquiries into internal systems clearly, timely, and compliantly
  • Perform checks on safety reports and medical enquiries
  • Write high-quality custom medical responses using client-approved resources
  • Provide informal training or mentorship to new team members
  • Contribute to process improvements and suggest updates to internal procedures
  • Participate occasionally in rotating after-hours coverage based on business needs

Requirements

What you’ll need
  • Degree in life sciences or a healthcare-related field
  • Strong written and verbal communication skills
  • High attention to detail and commitment to accuracy
  • Interest in drug safety, medical information, or regulatory affairs
  • Proactive mindset and willingness to learn
  • C1 fluency in Swedish and English, written and oral
  • Ability to occasionally participate in rotating after-hours coverage

Benefits

Comp & perks
  • Remote working support
  • Hybrid working encouraged for new hires near an office
  • Diversity, equity, and inclusion commitment
  • Equal Opportunity Employer
  • Safe and empowering workplace