Biomapas

Pharmacovigilance Specialist (Case Processing)

Croatia full-time Mid Salary not listed
full-time Mid level Technology & IT Curated
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About the role

The Pharmacovigilance Specialist will be responsible for ensuring the operational delivery of assigned tasks at the project level, with a focus on safety case reporting, processing of safety case report data, and literature screening activities. The role involves communication with the Pharmacovigilance Team Leader and Pharmacovigilance Manager regarding potential risks related to operational delivery, quality standards, client relationships, and the company's reputation, as well as addressing ad hoc project tasks and requirements.
CV must be in English language for further assessment.
Position is full-time remote/home-based in any European country and Turkey.
Responsibilities:

Oversee and manage the workflow of safety case reports, ensuring efficient processing

Perform triage on safety case reports to assess priority and necessary actions

Review, manage, and file source documentation in compliance with regulatory requirements

Process safety case reports, including SDB data entry, narrative writing, seriousness assessment, medical review (including causality and expectedness assessments), and reporting requirements evaluation

Conduct follow-up activities and manage queries related to safety case reports

Execute quality control checks on data entry and case processing to ensure accuracy and compliance

Reconcile safety case reports to ensure consistency and completeness of data

Prepare line listings to summarize and report on safety case data

Requirements

University degree in Life Science field

At least 1 year of experience in Safety and Pharmacovigilance within the pharmaceutical or Contract Research Organization (CRO) industry

Experience of clinical trial case processing in a safety database.

Proficiency in both verbal and written local language and English

Strong expertise with MS Office

Beneficial experience with Veeva Vault Safety system

Knowledge of EU GVP modules and applicable global safety regulations (e.g. ICH, FDA reporting requirements)

Benefits

Full remote flexible work

Professional growth and career opportunities

International team and environment

Originally posted on Himalayas

Interview prep

Walk in with sharper answers.

Use this as a quick practice sheet before you speak with the employer.

Mid
Technology & IT Data Analysis Remote Collaboration SQL Writing Mid level full-time

Likely questions

  1. Tell us about work you have done that is close to the Pharmacovigilance Specialist (Case Processing) role.
  2. How would you approach your first 30 days at Biomapas?
  3. Which of Data Analysis, Remote Collaboration and SQL have you used recently, and what did it help you achieve?
  4. Describe a time you solved a problem without waiting to be told exactly what to do.
  5. How do you handle busy days, changing priorities, or pressure at work?

Prepare before the call

  • A recent example that proves your experience with Data Analysis, Remote Collaboration and SQL.
  • One short story with a problem, your action, and the result.
  • Two examples that show the strengths listed on your CV.
  • A clear reason why this role and company interest you.
  • Your availability, preferred work style, and salary expectations.

Ask them

  • What would success look like in the first 90 days?
  • What are the main problems this hire should help solve?
  • How does the team give feedback and measure good work?
  • What does a normal working week look like for this role?
Practice line

I am interested in the Pharmacovigilance Specialist (Case Processing) role because I can bring practical experience in Data Analysis, Remote Collaboration and SQL, learn the team quickly, and contribute to the outcomes Biomapas needs from this hire.

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