3 - 8 years

2 - 5 Lacs

Posted:5 hours ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

Roles and Responsibility
  • Develop high-quality medical documents, including clinical trial protocols, informed consent forms, and case study reports.
  • Review and edit medical documents for accuracy, clarity, and compliance with regulatory requirements.
  • Collaborate with cross-functional teams, including clinicians, researchers, and statisticians, to ensure timely delivery of documents.
  • Conduct thorough reviews of documents to identify areas for improvement and implement changes as needed.
  • Stay up-to-date with industry trends and developments in medical research and technology.
  • Participate in document development activities, including creating templates, guidelines, and standard operating procedures.
Job Requirements
  • Minimum 3 years of experience in medical writing or a related field.
  • Strong knowledge of medical terminology, regulations, and standards (e.g., GCP, ICH).
  • Excellent written and verbal communication skills, with the ability to communicate complex information clearly.
  • Strong analytical and problem-solving skills, with attention to detail and the ability to work independently.
  • Ability to manage multiple projects simultaneously and meet deadlines.
  • Familiarity with document management systems and software applications (e.g., Word, Excel, PowerPoint).

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