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Pharmacovigilance Officer

Excelya

Paris

Sur place

EUR 45 000 - 65 000

Plein temps

Il y a 3 jours
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Résumé du poste

A mid-size CRO in Paris seeks a Pharmacovigilance professional to supervise case management, ensuring compliance and data integrity. The ideal candidate possesses a Doctor of Pharmacy (PharmD) and thrives in collaborative environments. Fluency in English and French is essential. The company values employee growth and encourages an ambitious, audacious approach to healthcare solutions.

Qualifications

  • Proven ability to thrive in collaborative, fast-moving environments.
  • Experience in managing CAPAs, deviations, and regulatory compliance indicators.
  • Fluent in written and spoken English and French.

Responsabilités

  • Supervise pharmacovigilance case management outsourced to assigned platform(s).
  • Respond to case-related emails and inquiries from external service providers.
  • Monitor case processing timelines and investigate any delays in reporting.
  • Support the review of clinical study case narratives for reports.
  • Collaborate with cross-functional teams to ensure compliance and data integrity.

Connaissances

Collaborative working
Understanding of global PV regulations
Managing CAPAs
Regulatory compliance indicators
Strong communication skills

Formation

Doctor of Pharmacy (PharmD)
Description du poste

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Pharmacovigilance. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main Responsibilities
  • Supervise pharmacovigilance case management outsourced to assigned platform(s)
  • Respond to case-related emails and inquiries from external service providers
  • Monitor case processing timelines and investigate any delays in reporting or transmission
  • Participate in weekly quality control of data entry, MedDRA coding, and narrative writing
  • Support the review and validation of clinical study case narratives for inclusion in study reports
  • Contribute to the reconciliation of PV cases with business partners per Safety Data Exchange Agreements (SDEAs)
  • Oversee reconciliation of cases with clinical databases managed by outsourced providers
  • Collaborate closely with cross-functional and global teams to ensure compliance and data integrity
Requirements

At Excelya, taking audacious steps is encouraged, so we're looking for individuals who are ready to grow with us and share our values.

  • Experience : Proven ability to thrive in collaborative, fast-moving environments (talent matters most to us!)
  • Skills : Solid understanding of global PV regulations and quality systems, experience in managing CAPAs, deviations, and regulatory compliance indicators, familiar with the preparation and conduct of audits and inspections (internal and external).
  • Education : Doctor of Pharmacy (PharmD) degree required.
  • Languages : Fluent in written and spoken English and French; strong communication skills with global teams.
Benefits
Why Join Us?

At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.

We are a young, ambitious health company representing 900 Excelyates, driven to become Europe's leading mid-size CRO with the best employee experience. Our one-stop provider service model offering full-service, functional service provider, and consulting enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient's journey.

Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.

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