Clinical Scientist Role

We are seeking a Clinical Scientist to support the design and development of clinical study protocols, endpoints, and criteria. This role involves translating research and product goals into evidence-generating study plans and partnering to execute studies that ensure alignment between scientific intent and operational delivery.

Key Responsibilities

• Support the design and development of clinical study protocols and endpoints.
• Translate research and product goals into evidence-generating study plans.
• Partner to execute studies ensuring alignment between scientific intent and operational delivery.
• Build relationships with internal teams, investigators, and external partners.
• Prepare study documents including protocols, investigator brochures, clinical study reports, and regulatory submissions.
• Ensure GCP compliance and alignment with data collection strategy.
• Utilize statistical methods or programming in Python or R.

Required Skills & Qualifications

• 5+ years in clinical research or scientific roles in medical devices.
• Strong analytical and problem-solving skills with data interpretation.
• Familiarity with clinical study design, endpoints, and data analysis concepts.
• Working knowledge of GCP and ISO 14155.
• Ability to work cross-functionally with clinicians, engineers, and operational teams.
• Opportunity to work with leading experts from multiple fields.
• Growth potential and fast-track advancement.