Clinical Scientist

Stevenson Search Partners

United States

On-site

USD 120,000 - 180,000

Full time

14 days+
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Job summary

Senior Clinical Development Scientist at Stevenson Search Partners partnered with a medical device client focused on innovating artificial fibrillation and developing next generation cardiac ablation systems.

The role leads global clinical studies, data analysis, and cross-functional collaboration with R&D, Regulatory Affairs, and KOLs to advance new cardiac technologies.

Qualifications

  • MS/PhD/MD or equivalent in Life Sciences, Medicine, Biomedical Engineering, or related field.
  • 3+ years of Clinical Development experience within medical devices.
  • Experience with Class III cardiovascular.
  • Cross-functional experience partnering with R&D and Regulatory Affairs.
  • Experience with clinical data analysis tools (MATLAB, Python, SAS, Minitab).

Responsibilities

  • Lead design, initiation, execution, and oversight of pre-market and post-market clinical trials for next-generation cardiac ablation technologies.
  • Develop and execute clinical strategy, development plans, and EU MDR clinical evaluations.
  • Oversee clinical data analysis to generate robust scientific evidence and insights.
  • Serve as internal scientific expert in cardiac electrophysiology and ablation technologies.
  • Collaborate with KOLs, clinical investigators, and physician advisors; represent the company at scientific conferences.
  • Drive publication strategy and physician education to support product adoption.

Skills

Cross-functional collaboration
Clinical development experience

Education

MS/PhD/MD or equivalent in life sciences/medicine/biomedical engineering

Tools

MATLAB
Python
SAS
Minitab

Job description

Our On-Demand Talent Solutions team is excited to announce an opportunity for a Senior Clinical Development Scientist to join our medical device client, whose primary focus is innovating artificial fibrillation and developing next generation cardiac ablation systems.

Summary: This individual will play a key role in shaping clinical strategy, designing and executing global clinical studies, analyzing clinical data, and partnering cross-functionally with R&D, Regulatory Affairs, Clinical Operations, Marketing, and Key Opinion Leaders to advance the company's next generation of products.

Responsibilities:

  • Lead the design, initiation, execution, and oversight of pre-market and post-market clinical trials, including pivotal studies for next-generation cardiac ablation technologies.
  • Develop and execute clinical strategy, clinical development plans, and EU MDR clinical evaluations supporting cardiac ablation catheters and PFA generators.
  • Oversee clinical data analysis to generate robust scientific evidence and meaningful clinical insights while supporting health economics and outcomes research initiatives.
  • Serve as the internal scientific expert in cardiac electrophysiology, atrial fibrillation, and cardiac ablation technologies, providing clinical input into product development documentation, IFUs, and technical materials.
  • Partner with Key Opinion Leaders (KOLs), clinical investigators, and physician advisors while representing the company at scientific conferences, advisory boards, and industry meetings.
  • Drive publication strategy, scientific communications, physician education, and product adoption through the interpretation and communication of clinical data.

Qualifications:

  • MS, PhD, MD, or equivalent in Life Sciences, Medicine, Biomedical Engineering, or related field.
  • 3+ years of Clinical Development experience within medical devices.
  • Experience with Class III cardiovascular.
  • Cross-functional experience partnering with R&D and Regulatory Affairs.
  • Experience with clinical data analysis tools (MATLAB, Python, SAS, Minitab).
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