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Freelance Medical Writer
2 weeks ago
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.