Clinical Trial Design Specialist

Clinical Trial Design Specialist
  • posted job: 2025-07-07
  • Florence
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  • Job Country: Italy
  • Job Industry: Biotechnology & Life Sciences
  • Job Profile: Product Development Scientist
  • Training Duration: Not Required
  • Number of Jobs Opening: 30
  • Salary: 3100 ( 3100 Per Month)
  • Job Type: Full Time
  • Visa: Provided by company
  • Food: Provided by company
  • Accommodation: Provided by company
  • Air ticket: Provided by company
  • Medical Insurance: Provided by Company
  • Commuting to job location: Provided by company
  • Required Experience: Not Required
  • Minimum Education Level: Not Required
  • Employee Acceptance: International
  • Work Location: Work at Office/Being at Work
  • Hiring Need: Immediate

Job Description:

Job Title: Clinical Trial Design Specialist
Location: Florence, Italy
Industry: Biotechnology & Life Sciences

Job Description:
We are looking for a motivated and skilled Clinical Trial Design Specialist to join our team in Florence, Italy under the Biotechnology & Life Sciences sector. In this role, you will be responsible for designing scientifically robust clinical studies that comply with regulatory and ethical standards. The ideal candidate should have expertise in clinical trial protocols, study design methodologies, and statistical planning. Key duties include preparing trial designs, selecting appropriate endpoints, calculating sample sizes, and working with biostatisticians and clinical teams. You will also contribute to IRB/ethics submissions and support the development of study documentation. This position requires scientific accuracy, regulatory understanding, and strategic thinking. It offers a key role in shaping the success of clinical research in Florence.

Job Requirement:

We are seeking a capable and enthusiastic individual for the role of Clinical Trial Design Specialist in Florence, Italy under the Biotechnology & Life Sciences sector. The ideal candidate should demonstrate experience in clinical study planning and medical research. Key requirements include:
• Knowledge of trial design principles and GCP guidelines
• Experience in writing and reviewing clinical protocols
• Understanding of statistical planning and clinical endpoints
• Strong project coordination and documentation skills
• Ability to work with cross-functional research teams
This role is ideal for detail-oriented professionals passionate about designing effective, ethical, and impactful clinical trials. We welcome qualified candidates to lead clinical planning in Florence.

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