Remote Principal Clinical Scientist, Diagnostics

Jobgether; United States; On-site; USD 130,000 - 150,000; Full time

Benefits offered by this job

Fully remote work

Bonus eligibility

Medical, dental, and vision insurance

Job summary

Jobgether, on behalf of a partner company, is seeking a Principal Clinical Scientist based in the United States to lead clinical trial strategies supporting diagnostic products across the US and EU markets.

This high-impact role generates robust clinical evidence for regulatory submissions and product commercialization, shapes study designs, protocols, evidence plans, and clinical claims while collaborating with Regulatory, R&D, Medical Affairs, Quality, and external experts while mentoring

Qualifications

• 9+ years of relevant clinical research experience, including US/EU trial experience
• Deep understanding of clinical study design and methodology in diagnostics/medical devices/pharma
• Strong ability to review, interpret, and communicate clinical trial data
• Excellent written and verbal communication with cross-functional teams
• Remote-work capable with cross-functional collaboration
• Travel up to 10% including overnight travel in US/EU

Responsibilities

• Design and execute clinical study strategies and evidence plans for regulatory submissions
• Develop protocols, claims, and evidence strategies with stakeholders and regulators
• Act as scientific liaison to regulators and external scientific audiences
• Collaborate with R&D, Regulatory, Medical Affairs, Quality, and Commercial teams
• Provide scientific oversight for study reports, technical files, and publications
• Mentor junior scientists and maintain knowledge of regulatory guidelines

Job description

Jobgether, on behalf of a partner company, is seeking a Principal Clinical Scientist based in the United States to lead clinical trial strategies supporting diagnostic products across the US and EU markets.

This high-impact role generates robust clinical evidence for regulatory submissions and product commercialization, shapes study designs, protocols, evidence plans, and clinical claims while collaborating with Regulatory, R&D, Medical Affairs, Quality, and external experts while mentoring