Requirements: English
Company: Excelya
Region: france, fr ,
We are a young, ambitious health company representing 900 Excelyates, driven to become Europes leading mid-size CRO with the best employee experience. Our one-stop provider service model offering full-service, functional service provider, and consultingenables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patients 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. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. 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. Objectives: Supervision of pharmacovigilance (PV) case management outsourced to two service providers. General Description of Responsibilities The consultant will oversee pharmacovigilance case management, including: Supervision of Outsourced Case Processing Responding to emails from service providers regarding case management. Weekly Quality Control (QC) of Case Processing Generating listings and verifying data consistency against source documents. Medical review of oncology cases. Experience with contract drafting, SDEAs, and oversight of third-party vendors, Strong background in international pharmacovigilance project coordination. ~ Degree in Life Sciences, Pharmacy, or Project Management ~ Fluency in French English