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Pharmacovigilance Case Processing Job (ProPharma)

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If you’re looking to grow your career in pharmacovigilance with a global leader, the Pharmacovigilance Specialist – Case Processing role at ProPharma is an excellent opportunity. This full-time position focuses on ICSR case processing, MedDRA coding, safety assessment, and regulatory compliance—ideal for candidates with strong attention to detail and a passion for patient safety.

ProPharma has spent 20+ years empowering biotech, pharma, and medical device companies across the product lifecycle. This is your chance to join a world-class PV team shaping the future of drug safety.


🔹 Key Responsibilities

As a Pharmacovigilance Specialist, you will be responsible for:

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  • Daily case processing of adverse event reports (clinical trial & post-marketing).
  • MedDRA coding, seriousness assessment, expectedness determination.
  • Preparing and reviewing case narratives.
  • Performing follow-up activities to collect additional safety information.
  • Sending client notifications based on case management requirements.
  • Supporting creation and delivery of training materials.
  • Escalating discrepancies to senior PV staff and managers.
  • Maintaining up-to-date knowledge of global safety regulations.
  • Conducting peer review of cases for accuracy and consistency.
  • Handling other PV-related duties as assigned.

🔹 Required Qualifications

Education

  • Required: Bachelor’s degree in Life Sciences.
  • Preferred: PharmD, MPharm, RPh, RN, or relevant advanced degree.

Experience

  • Minimum 2 years of experience in pharmacovigilance or safety case processing.

Skills

  • Strong written & verbal communication.
  • High attention to detail.
  • Ability to troubleshoot and resolve issues.
  • Strong organizational, time management, and multitasking skills.
  • Ability to work independently and cross-functionally.
  • Basic understanding of pharmacovigilance principles and regulations.

🔹 Benefits of Working at ProPharma

  • Opportunity to work with a global leader in drug safety.
  • Inclusive, diverse, and supportive workplace culture.
  • Career development through training and advanced PV exposure.
  • Collaborative, innovation-driven work environment.
  • Transparent application experience—every applicant receives a response.

🔹 How to Apply

Application Link

Pharmacovigilance Case Processing Job (ProPharma)
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