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Local Contact Person for Pharmacovigilance (Freelance - Part Time) - Remote

Posted 3 days ago
All others
Part Time
Estonia

Overview

The Local Contact Person for Pharmacovigilance (LCPPV) coordinates and performs the logistical aspects of pharmacovigilance activities in post-marketed programs to ensure compliance with local requirements.

In Short

  • Building a network of PV experts for freelance opportunities.
  • Part-time freelance role focusing on pharmacovigilance.
  • Coordinates operational pharmacovigilance activities.
  • Acts as a primary contact for local regulatory authorities.
  • Monitors safety issues and local legislation changes.
  • Supports client audits and inspections.
  • Performs local literature screening.
  • Assists in the development of local pharmacovigilance documentation.
  • Manages risk minimization measures locally.
  • Provides training and activity reports on local PV systems.

Requirements

  • Experience in pharmacovigilance and regulatory compliance.
  • Strong communication skills for liaising with authorities.
  • Ability to monitor and report on safety issues.
  • Familiarity with local legislation and PV practices.
  • Experience with client audits and inspections.
  • Proficient in literature screening and safety information collection.
  • Experience in training personnel in pharmacovigilance.
  • Ability to provide detailed monthly activity reports.

Benefits

  • Flexible work schedule as a freelance role.
  • Opportunity to work with a dedicated team.
  • Engagement in meaningful projects within biopharmaceuticals.
  • Collaboration with various professionals in the industry.
  • Potential for ongoing freelance opportunities.
Allucent logo

Allucent

Allucent™ is a dedicated partner for small to medium biopharmaceutical companies, specializing in guiding them through the complexities of clinical trials. With a focus on delivering life-changing therapies to patients globally, Allucent provides comprehensive project administration and support services to ensure projects are completed within budget and on time. The company fosters a collaborative and flexible work environment, offering opportunities for professional development and internal growth, while maintaining a commitment to quality and regulatory standards in drug development and clinical research.

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