Seeking Exceptional Senior Medical Writer to Join Innovative Team Are you an experienced medical writer ready to make a significant impact in the pharmaceutical industry?
We're looking for a talented professional to join our growing, innovative team focused on driving excellence in regulatory documentation.
Key Requirements: 7-8+ years of experience in clinical medical writing within the pharmaceutical industry Proven expertise in writing regulatory documents including CSRs, IBs, Protocols, Summaries, and NDA/BLA/MAA submissions Strong scientific background with a degree in life sciences or related field (Master's or PhD preferred) Excellent communication skills and ability to collaborate effectively in cross-functional teams Ideal Candidate: Experience in Immunology, Pulmonology, or Neuroscience therapeutic areas Ability to write and edit all clinical regulatory documents, including complex deliverables like Briefing Books and Paediatric Plans Proactive problem-solver with a talent for driving project consensus Eager to learn and grow within a dynamic team environment Key Responsibilities: Author and edit high-quality clinical regulatory documents Oversee outsourced writing deliverables and manage resources effectively Maintain document timelines and ensure adherence to regulatory guidelines Mentor junior staff and provide strategic support at the product level Participate in document team and clinical sub-team meetings Contribute to process improvements and SOP development We offer a seamless, work-focused culture that encourages innovative ideas.
Join us in our mission to make a difference in patients' lives.
If you're ready to take your medical writing career to the next level in a challenging and rewarding environment, we want to hear from you.
Apply now and be part of our exciting future in pharmaceutical innovation.