0 - 5 years

1 - 5 Lacs

Posted:1 day ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

Roles and Responsibility
  • Conduct thorough medical reviews of device-related documents, including clinical trial protocols and study reports.
  • Collaborate with cross-functional teams to ensure compliance with regulatory requirements and industry standards.
  • Develop and maintain expertise in medical devices and equipment, staying up-to-date on new technologies and trends.
  • Provide guidance and support to junior staff members, sharing knowledge and best practices.
  • Participate in quality improvement initiatives, identifying areas for process enhancement and implementing changes.
  • Maintain accurate records of all interactions with clients, including phone calls, emails, and written correspondence.
Job Requirements
  • Strong understanding of medical terminology, regulations, and guidelines related to medical devices.
  • Excellent analytical and problem-solving skills, with attention to detail and the ability to interpret complex data.
  • Effective communication and interpersonal skills, enabling collaboration with diverse stakeholders.
  • Ability to work independently and as part of a team, demonstrating flexibility and adaptability.
  • Proficiency in using electronic health records systems and other healthcare software applications.
  • Commitment to ongoing learning and professional development, staying current with industry advancements.

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