Pharmacovigilance Coordinator (M/F)

At APLUSA, we are convinced that a better understanding of health allows for better decision-making for both patients and healthcare professionals. Every day, our teams transform data into useful and concrete insights to help healthcare stakeholders better understand field realities, support innovation, and improve care pathways.

But what truly makes APLUSA is, above all, our more than 160 international employees: passionate, curious, and committed men and women, evolving in a stimulating environment.

Joining APLUSA means putting your energy and intelligence at the service of meaningful work, and growing within a company where high standards, humanity, and utility move forward together.

Become an Aplusien.ne!

Your missions:

Under the supervision of the Pharmacovigilance Manager, you will ensure the administrative follow-up of pharmacovigilance for quantitative studies conducted by A+A within the France and International scope.

In this context, your missions will consist of:

• Actively participating in study kick-off meetings,
• Processing respondent data and identifying Vigilance cases (notably pharmacovigilance and quality complaints),
• Acting as the point of contact for laboratories for the transmission of identified cases
• Ensuring the construction and follow-up of the reconciliation table,
• Taking charge of quality controls
• Verifying the accuracy of files and managing their archiving.
• Carrying out training follow-up
• Supporting internal or external personnel on training
• Ensuring the exchange of information internally and externally
• Using technological tools dedicated to pharmacovigilance to secure case follow-up, reconciliation, archiving, and quality controls,
• Relying on AI assistants, in compliance with internal policy, to support the performance of missions.
• You may also be required to participate in any action to improve the Pharmacovigilance service or your Department (documentary updates, creation of e-learning courses, implementation of CAPAs, process improvement, etc.).

Your profile:

• From a higher education background at the bac+2/3 level in Pharmacovigilance (type ENCPB, etc.), Regulatory, Health, or Quality, you ideally have a first experience in a company.
• You demonstrate a real interest in the Health/Pharmaceutical field and master the Pack Office (PowerPoint and Excel).
• You have an appetite for digital tools, AI solutions, and continuous process improvement, with the desire to use them in a pragmatic and secure manner to gain efficiency and reliability.
• You are recognized for your interpersonal skills and communication abilities, both oral and written. You are autonomous, organized, rigorous, methodical, and committed to your missions.
• Your natural curiosity and your analytical and team spirit will allow you to successfully carry out your mission.

As we are an international company, you must have good written and spoken English.

Our benefits:

Remuneration according to profile Holiday bonus 11 RTT Teleworking Flexible hours Restaurant vouchers Mutual insurance and contingency plan Lifelong training for the employee