Clinical Trials Coordinator

Clinical Trials Coordinator
  • posted job: 2025-07-07
  • Rome
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  • Job Country: Italy
  • Job Industry: Biotechnology & Life Sciences
  • Job Profile: Clinical Research Associate
  • Training Duration: Not Required
  • Number of Jobs Opening: 49
  • Salary: 2700 ( 2700 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 Trials Coordinator
Location: Rome, Italy
Industry: Biotechnology & Life Sciences

Job Description:
We are looking for a motivated and skilled Clinical Trials Coordinator to join our team in Rome, Italy under the Biotechnology & Life Sciences sector. In this role, you will be responsible for managing the daily operations of clinical studies, ensuring compliance with regulatory requirements and timelines. The ideal candidate should have a good understanding of clinical research protocols, patient enrollment procedures, and data management systems. Key duties include coordinating with investigators and sponsors, maintaining study documentation, monitoring trial progress, and ensuring ethical standards are upheld throughout the study. You will also assist with site training and audit preparation. This position requires strong organizational skills, attention to detail, and excellent communication abilities. This is a unique opportunity to support innovative clinical research projects in Rome.

Job Requirement:

We are seeking a capable and enthusiastic individual for the role of Clinical Trials Coordinator in Rome, Italy under the Biotechnology & Life Sciences sector. The ideal candidate should demonstrate familiarity with clinical research operations. Key requirements include:
• Experience in managing or supporting clinical trials
• Strong knowledge of GCP (Good Clinical Practice) and ICH guidelines
• Excellent documentation and communication skills
• Ability to coordinate with cross-functional teams and external partners
• Detail-oriented mindset with a commitment to patient safety and data integrity
This role suits individuals passionate about advancing medical science through structured and compliant research. We welcome candidates ready to ensure quality and efficiency in clinical trial operations in Rome.

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