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Ergomed

Runs clinical trials and monitors drug safety

Senior Pharmacovigilance Associate

Biology & BiotechConfirmed live in the last 24 hours
Full-timeZagreb, CroatiaNo salary listedHybrid

About the Job

Requirements

  • A life science graduate, pharmacy, nursing, another healthcare-related qualification, or experience in pharmacovigilance is required.
  • At least 1 year of work experience in pharmacovigilance is required.
  • Organization skills, including attention to detail and multitasking, are required.
  • Management skills, including time and issue management, are required.
  • Advanced spoken and written English is required.
  • Advanced literacy in Microsoft Office is required.

Responsibilities

  • Process Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations, PrimeVigilance procedures, client-specific requirements, and timelines.
  • Perform ICSR follow-up.
  • Manage serious adverse events (SAEs) and suspected unexpected serious adverse reactions (SUSARs), including unblinding, clinical trial reconciliation, protocol review, and Safety Management Plan review.
  • Perform clinical and partner reconciliation.
  • Protect personal data.
  • Handle Product Quality Complaints and interact with Quality Assurance.
  • Interact with Medical Information.
  • Perform MedDRA and WHO coding.
  • Prepare database outputs and reports, including data for monthly client reporting.
  • Manage workflow and resources.
  • Support pharmacovigilance processes related to ICSR management within PrimeVigilance and for clients.
  • A more senior colleague may perform tasks assigned by standard operating procedures to a more junior position.
  • Support the Regulatory Affairs and Pharmacovigilance Network Department as needed, including acting as the Local Contact Person for Pharmacovigilance for the specified country and as the Person Responsible for Local Screening for the designated language, as agreed with the line manager.

About the Company

Ergomed

Runs clinical trials and monitors drug safety

Ergomed manages clinical trials and drug safety for biotechnology and pharmaceutical companies, with a focus on complex cancer and rare-disease studies. Its clinical research business supports development from early testing through studies after approval, with services adapted to difficult patient populations. Teams plan trials, recruit patients, monitor study sites, and analyze results under paid service contracts. PrimeVigilance tracks medicine safety and answers medical inquiries, while ADAMAS Consulting advises clients on quality and regulatory compliance across drug development. Ergomed was founded in 1997 and has its global headquarters in Guildford, Surrey, United Kingdom.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Guildford, United Kingdom
Founded
1997

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