Medical Content Developer

vor 1 Monat


Zug, Zug, Schweiz PSI Vollzeit

Key Responsibilities

  • Develop and maintain high-quality clinical documentation for research projects, ensuring accuracy and completeness.
  • Review and finalize clinical study reports, including patient safety narratives, to ensure compliance with regulatory requirements.
  • Collaborate with Quality Assurance teams to ensure documentation meets quality standards.
  • Analyze and summarize data from clinical studies to inform documentation.
  • Stay up-to-date on relevant scientific literature and regulatory guidelines.
  • Conduct quality control reviews of clinical documentation to ensure accuracy and consistency.
  • Support cross-functional teams, including Project Managers and Process Improvement teams, with medical writing tasks.

Requirements

  • Bachelor's or Master's degree in biomedical or life sciences.
  • At least 2 years of industry experience in clinical documentation.
  • Experience in pharmaceutical, biotechnology, or contract research organizations.
  • Knowledge of global regulations and guidelines in drug development.
  • Familiarity with electronic Common Technical Document requirements.

About PSI

PSI is a leading company in the field of clinical research and drug development, dedicated to delivering high-quality solutions that make a difference in the lives of patients worldwide.



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