Clinical Evidence Planning and Evaluations Manager

At-a-Glance:

Are you ready to build your career by joining a multi-national medtech company? If so, our client is hiring a Clinical Evidence Planning and Evaluations Manager.

Position Type:

• Contract
• Remote
  
  
  

Required:

• Master's or PhD in Medical Physics (preferred), Biophysics, Biomedical Engineering. Other degree programs considered based on experience.
• 2-5 years' experience with clinical evaluations, medical physics, or related field.
• Familiarity with design and manufacture medical devices, especially those used in the radiation oncology setting.
• Exemplary technical writing and verbal communication skills.
• Understanding of Clinical Evaluation and Post Market Clinical Follow Up Requirements of class I-III medical devices as designated in the European Union Medical Device Regulation (EU MDR).
  
  
  

Responsibilities:

• Creating and driving the Clinical Evidence Strategy for Varian's devices.
• Creation of Clinical Evaluation Plans, Reports, and Post-Market Clinical Evaluation Plans, and Reports (CEP/CER and PMCFP/PMCFR).
• Providing clinical perspective and input to cross-functional teams regarding clinical development, risk management, product management, and post-market surveillance.
• Execute Post-Market Clinical Follow Up activities (may include customer surveys, annual literature searches, and clinical studies).
• Provide clinical review of promotional material and claims in support of publishing customer facing content.
  
  
  

Get in Touch:

We want to hear from you! If you think you'd be a good match, submit your resume and reach out to Komal at 862-390-7418 to learn more.

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