Parexel is looking for an experienced Regulatory Affairs Consultant to join our team on a client dedicated project. The role can be office or home based in various European locations, with a focus on post-approval CMC activities for biological and plasma products. You will develop submission strategies, assess change controls, coordinate submissions, and manage regulatory information systems to ensure timely global submissions and regulatory compliance. #J-18808-Ljbffr
Remote Regulatory Affairs Consultant - CMC & Post-Approval employer: PAREXEL
At Parexel, we pride ourselves on being an exceptional employer, offering a collaborative work culture that fosters innovation and professional growth. Our team members enjoy competitive benefits, including flexible working arrangements and opportunities for career advancement, all while contributing to impactful global clinical trials in a supportive environment across the UK, Poland, Serbia, and Hungary.
