Medical Content Developer
vor 1 Monat
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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