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Sonova AG

Senior Clinical Evaluation Specialist (m/f/d)

London
Posted 22 days ago
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Advanced Bionics | Clinical Research

Germany or UK - Full remote or Hybrid in Hannover office

At Advanced Bionics, a Sonova brand, we are passionate about transforming lives through innovative hearing solutions. As a Senior Clinical Evaluation Specialist, you will play a key role in generating and communicating clinical evidence that supports the safety, performance, and regulatory compliance of our cochlear implant technologies.

Your Responsibilities

  • Independently author and maintain Clinical Evaluation Plans (CEP), Clinical Evaluation Reports (CER), SSCPs, and PMCF documentation
  • Conduct systematic literature reviews, including evidence appraisal and data synthesis
  • Identify clinical evidence gaps and recommend appropriate data generation strategies
  • Support regulatory submissions and responses to Notified Bodies and regulatory authorities
  • Plan and execute PMCF activities, including study coordination, data analysis, and reporting
  • Collaborate with Regulatory Affairs, Clinical Research, Quality, and other cross-functional stakeholders
  • Ensure all clinical evaluation deliverables meet the highest scientific and regulatory standards

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I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?

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Graduate Consultant — 2026 Scheme

PwC·London, UK
£35,000/yr

Why you're a good match

Strong

Your economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.

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Why you're a good match

You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.

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Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.

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What You Bring

  • Master's degree in a clinical or life sciences field such as Audiology, Biomedical Engineering, Medicine, Pharmacy, Nursing, Public Health, or a related discipline
  • At least 2 years of experience in clinical evaluation, medical writing, or clinical research within the medical device industry
  • Proven experience authoring Clinical Evaluation Plans (CEP) and Clinical Evaluation Reports (CER)
  • Strong knowledge of systematic literature reviews, clinical evidence appraisal, and scientific writing
  • Excellent analytical skills with the ability to interpret and synthesize clinical data
  • Strong organizational skills and the ability to manage multiple priorities independently
  • Fluent English communication and scientific writing skills

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What We Offer

  • The opportunity to contribute to life-changing hearing technologies
  • A collaborative and international working environment
  • Exposure to innovative research and cutting-edge medical devices
  • Flexible working arrangements and opportunities for professional development
  • A culture that values ownership, scientific excellence, and continuous learning

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Location

London, England, United Kingdom

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