Senior Clinical Development Scientist (Ultras

ZipRecruiter; Cambridge; Hybrid; GBP 70,000 - 90,000; Full time

Job summary

Join a leading team committed to revolutionizing ultrasound technology as a Senior Clinical Development Scientist. In this role, you will lead clinical studies, develop essential documentation, and collaborate with various stakeholders to ensure regulatory success and optimal patient outcomes. We offer a competitive salary and plenty of opportunities for professional growth.

Benefits

Competitive salary

Opportunities for growth

Benefits package

Qualifications

• 7+ years in clinical research or development, preferably with medical devices.
• Strong experience designing clinical studies for regulatory environments.
• Excellent writing and communication skills in English.

Responsibilities

• Design and lead clinical studies for ultrasound products.
• Develop regulatory documentation for FDA and international submissions.
• Collaborate with cross-functional teams and analyze clinical data.

Skills

Clinical research

Regulatory documentation

Communication skills

Data analysis

Education

PhD or MD in a relevant scientific field

Job description

Job Description

Location: Bothell, WA • Cambridge, MA • Plymouth, MN (Hybrid – 3 days onsite)

Are you a clinical science expert ready to impact the future of ultrasound technology? Join our innovative team as a Senior Clinical Development Scientist and lead the strategy, execution, and documentation of clinical studies that drive regulatory success and patient outcomes.

Key Responsibilities:

• Design and lead clinical studies (pre-market and post-market) for ultrasound products.
• Develop protocols, CSRs, CERs, and regulatory documentation to support FDA and international submissions.
• Collaborate with cross-functional teams (R&D, Regulatory, Medical Affairs, Market Access).
• Engage with investigators, IRBs, and global regulatory agencies (FDA, EMA, NMPA).
• Analyze clinical data, support health economics evidence, and drive publication strategy.

Ideal Candidate Has:

• PhD or MD in a relevant scientific field (required).
• 7+ years in clinical research or development, preferably with medical devices.
• Strong experience designing clinical studies for regulatory environments (FDA, EU-MDR).
• Solid understanding of GCP, design controls, and product development processes.
• Excellent writing and communication skills in English for scientific documentation.
• Experience with ultrasound and/or AI-driven clinical validation (a plus).
• Based near one of the required offices with ability to work onsite 3 days/week.

Why Join Us?

• Help shape the next wave of ultrasound innovation.
• Collaborate with thought leaders and make an impact globally.
• Competitive salary, benefits, and opportunities for growth.