Senior Medical Writing Director

14 hours ago


London, Greater London, United Kingdom atai Full time
Senior Medical Writing Manager

The Senior Medical Writing Manager will play a key role in the development of clinical trials for atai's innovative therapeutics. This individual will be responsible for designing and developing Phase 1-3 clinical trials, working closely with cross-functional teams to ensure the successful execution of these studies.

Key Responsibilities:
  • Drive the conceptualization and design of clinical development plans (CDPs) and clinical trials, ensuring alignment with atai's global strategy.
  • Collaborate with regulatory affairs, biometrics, safety, and operations teams to ensure high-quality protocol documents and effective study execution.
  • Provide medical expertise and oversight to project teams, ensuring the ethical and medical aspects of studies are met.
  • Contribute to the clinical components of Investigator Brochures (IBs) and documents for regulatory submissions.
  • Maintain scientific and clinical knowledge in relevant therapeutic areas and provide input across chapters as needed.
Requirements:
  • 5+ years of experience in drug development, preferably in neurology or psychiatry indications.
  • Board certification in psychiatry or a related field is preferred.
  • Active medical license is preferred.
  • Demonstrated expertise in clinical trial methodology, study design, and protocol writing.
  • Excellent communication and interpersonal skills, with the ability to distill complex issues into simple terms.

atai is a clinical-stage biopharmaceutical company dedicated to transforming the treatment of mental health disorders. We are seeking a highly skilled and innovative Senior Medical Writing Manager to join our team and contribute to the development of life-changing therapeutics.



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