Staff Clinical Evaluation Specialist in Gurgaon, भारत

Staff Clinical Evaluation Specialist responsible for developing clinical evidence strategies across product development cycles, preparing regulatory submissions, and conducting systematic literature reviews. Role requires coordination with marketing, regulatory, and research teams to establish device safety and performance documentation.

Responsibilities

• Develop and maintain clinical evidence strategy throughout product development lifecycle
• Prepare and update regulatory submissions including clinical evaluation reports and safety summaries
• Design and execute systematic literature searches to summarize published clinical evidence
• Review clinical documentation authored by peers and external contributors for compliance
• Identify unanswered clinical questions and support post-market surveillance activities

Requirements

• Bachelor's degree in technical or scientific discipline
• 7-10 years of professional experience
• Nursing degree or advanced practice clinical experience (critical care, emergency, flight nursing)
• Minimum 4 years medical device industry experience in clinical, quality, or regulatory affairs
• Ability to interpret regulations, technical standards, and complex medical documentation
• Project management experience and proficiency with scientific/medical writing