Freelance/Contract - Pharmacovigilance Specialist, Case Processing & QPPV Support

Job description

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. Position overview: ProPharma is currently supporting a global Life-sciences brand as their Pharmacovigilance department requires support for Case Processing and QPPV activities with in the EU. This position is offered as a one year project (Fixed term or freelance/Contract); it will offer 1.0 FTR (40 hours per week) and is to commence immediately. The role is required Hybrid working based out of Lund throughout the project and fluency in English and ideally Swedish (or another EU...