3 - 8 years

2 - 5 Lacs

Posted:13 hours ago| Platform: Naukri logo

Apply

Work Mode

Work from Office

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 physicians, researchers, and other stakeholders, to develop and review medical documents.
  • Conduct thorough reviews of medical 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 the development of new medical document templates and tools.
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).
  • Excellent written and verbal communication skills.
  • Ability to work independently and collaboratively as part of a team.
  • Strong analytical and problem-solving skills.
  • Familiarity with medical software applications and systems.
  • Educational qualification: Any Graduate or Postgraduate degree.

Mock Interview

Practice Video Interview with JobPe AI

Start Job-Specific Interview
cta

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.

Job Application AI Bot

Job Application AI Bot

Apply to 20+ Portals in one click

Download Now

Download the Mobile App

Instantly access job listings, apply easily, and track applications.

coding practice

Enhance Your Skills

Practice coding challenges to boost your skills

Start Practicing Now

RecommendedJobs for You