Clinical Safety Analyst (Medical Device)

3 - 7 years

1 - 4 Lacs

Posted:6 hours ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

Roles and Responsibility
  • Conduct thorough analysis of clinical trial data to identify potential safety risks and trends.
  • Develop and implement effective safety protocols and procedures to mitigate identified risks.
  • Collaborate with cross-functional teams, including regulatory affairs, quality assurance, and product development.
  • Prepare and review safety reports, such as adverse event reports and periodic safety update reports.
  • Stay up-to-date with changing regulations and guidelines related to clinical safety.
  • Provide training and guidance to internal stakeholders on clinical safety best practices.
Job Requirements
  • Strong understanding of clinical trials, safety protocols, and regulatory requirements.
  • Experience with medical devices or pharmaceuticals is preferred.
  • Excellent analytical, problem-solving, and communication skills.
  • Ability to work effectively in a fast-paced environment with multiple priorities.
  • Strong attention to detail and organizational skills.
  • Familiarity with quality management systems and ISO standards.
  • Educational qualifications: Any Graduate/Postgraduate degree.

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