Data Protection Analysts

2 days ago


Kanpur, Uttar Pradesh, India beBeePharmacovigilance Full time ₹ 9,00,000 - ₹ 12,00,000

We are seeking dynamic professionals to join our team as Pharmacovigilance Specialists.

As a key member of our pharmacovigilance team, you will be responsible for managing safety case receipt, processing, and data entry, quality control tracking, and ICSR follow-up for all safety information received from clients.

The ideal candidate will have a strong understanding of pharmacovigilance principles, adverse event reporting, and causality assessment. They will also possess excellent organizational and interpersonal skills, with the ability to work well within a team and communicate complex concepts effectively.

Our team is looking for individuals with a deep knowledge of pharmacovigilance regulations, including US and EU PV guidelines. A pharmaceutical background and experience working to deadlines are highly desirable.

  • Responsibilities include:
  • Performing local safety case receipt, processing, and data entry
  • Managing generic or client-specific email boxes
  • Registration, triage, assignment, and coordination of vigilance cases
  • Follow-up requests with local reporters
  • Responding to queries from clients and reporters
  • Carrying out periodic reconciliations to confirm proper handling of vigilance reports

Requirements:

  • Bachelor's or Master's degrees in Medicine, Pharmacy, Nursing, or Science-related field
  • 2+ years' experience in pharmacovigilance working for service providers
  • Previous experience working to deadlines and communicating with clients
  • Strong understanding of GVP, GCP, FDA, and regulatory requirements
  • Excellent time management and communication skills


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