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Freelance Medical Writer

2 weeks ago


Eastern England, United Kingdom i-Pharm Consulting Full time

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.