Clinical Scientist Role

New

Skills

Clinical protocols Clinical research Clinical study design Data collection strategy Endpoints development GCP compliance ISO 14155 Python programming R programming Statistical methods

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.

No forms. Your profile is generated instantly.

Job Type: Remote

Salary: Not Disclosed

Experience: Entry

Duration: Months

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