TFS HealthScience

Clinical Research Associate

TFS HealthScience

full-time

Posted on:

Origin:  • 🇩🇪 Germany

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Job Level

JuniorMid-Level

Tech Stack

Google Cloud PlatformTFS

About the role

  • Lead on-site and remote monitoring of clinical trials, ensuring data integrity, patient safety, and regulatory compliance
  • Initiate, monitor (on-site and remote), and close out study sites during clinical trials
  • Verify informed consent procedures and protocol compliance to protect participants
  • Review CRFs and source data to ensure accuracy and completeness
  • Oversee management and accountability of investigational products and maintain audit readiness
  • Document monitoring visit findings in detailed reports, escalate issues, and update tracking systems
  • Collaborate with sites to resolve findings, deliver action plans, and maintain Trial Master File (TMF)

Requirements

  • A degree in life sciences, nursing, or a related field
  • At least one year of clinical research experience or relevant academic background
  • Strong understanding of Good Clinical Practice (GCP), ICH guidelines, and basic medical terminology
  • Clear and professional communication skills
  • Excellent organizational abilities and attention to detail
  • Fluency in English and confidence using digital tools and systems
  • Flexibility, a proactive mindset, and willingness to travel up to 60–80%