Principal Clinical Scientist
Job Summary
Providing scientific leadership across global clinical development programs, the full-time remote Principal Clinical Scientist will lead clinical study design, regulatory strategy, and evidence generation to support innovative medical device technologies.
Key responsibilities
- Lead the scientific design and oversight of clinical studies from concept through publication
- Develop clinical study protocols, reports, and essential regulatory documents for submissions
- Collaborate with cross-functional teams to advance clinical development programs and support regulatory submissions
Required qualifications
- Master's degree in Life Sciences, Health Sciences, or a related scientific discipline
- Minimum 8 years of experience in clinical development, clinical research, or Medical Affairs
- Demonstrated experience in developing clinical study protocols and regulatory documents
- Strong knowledge of ICH-GCP, ISO 14155, and FDA regulations
- Ability to travel approximately 15-25% for scientific congresses and study-related activities
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