Parexel is seeking an experienced Regulatory Affairs Consultant CMC Author to support our client. The role focuses on CMC authoring for initial submissions and lifecycle management, with emphasis on biologics. The position can be home or office based across European locations, offering flexibility for experienced professionals. Qualified candidates have 10+ years in CMC and regulatory affairs, strong regulatory knowledge (ICH, EU/US), and experience with document management systems. #J-18808-Ljbffr
Senior CMC Regulatory Affairs Consultant (Biologics) 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.
