Medical Reviewer I

Ergomed

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profile Job Location:

Zagreb - Croatia

profile Monthly Salary: Not Disclosed
Posted on: 25-10-2025
Vacancies: 1 Vacancy

Job Summary

Responsibilities include:

  • To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness listedness / expectedness and Company causality as well as writing of Company comment follow-up questions and Analysis of Similar Events when required. Including completion of all required supporting documentation such as trackers.
  • To review literature screening search strategy
  • To review articles to determine if they contain ICSRs/SAEs related to the relevant Medicinal Product or other safety related findings
  • Reviewing database outputs
  • To review and provide input in Periodic Safety Update Reports
  • To review and provide input in Development Safety Update Reports
  • Participating in signal detection activities including meetings and writing signal detection reports
  • Proposing a course of action whenever a possible signal is identified

Qualifications :

  • Medically qualified as a physician with demonstrated experience in Pharmacovigilance
  • Any experience in aggregate reports and signal detection is desirable
  • Excellent interpersonal skills
  • Ability to plan organise prioritise and execute multiple tasks
  • Ability to work effectively cross culturally and cross functionally and value the importance of teamwork
  • Communication skills
  • Presentation skills

Additional Information :

We prioritize diversity equity and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds genders and ages can contribute and grow. 

To succeed we must work together with a human first approach. Why Because our people are our greatest strength leading to our continued success on improving the lives of those around us. 

 We offer: 

  • Training and career development opportunities internally 
  • Strong emphasis on personal and professional growth 
  • Friendly supportive working environment 
  • Opportunity to work with colleagues based all over the world with English as the companylanguage 

Our core values are key to how we operate and if you feel they resonate with you then PrimeVigilance could be a great company to join! 

  • Quality 
  • Integrity & Trust 
  • Drive & Passion 
  • Agility & Responsiveness 
  • Belonging 
  • Collaborative Partnerships 

Come and join us in this exciting journey to make a positive impact in patients lives. We look forward to welcoming your application!


Remote Work :

Yes


Employment Type :

Full-time

Responsibilities include:To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness listedness / expectedness and Company causality...
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Key Skills

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About Company

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Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance solutions, integrated under the PrimeVigilance brand and a full range of high-quality clinical research and trial management services under the Ergomed Clinical Research brand. ... View more

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