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.