CRA II / Senior CRA - remote working

CRA II / Senior CRA - remote working

Vollzeit Homeoffice
i‑Pharm Consulting

We are partnering with a well-established global CRO seeking a CRA II/Senior CRA to support both oncology and neurology studies across Germany. This is an excellent opportunity to join a high-performing clinical operations team where you'll manage site relationships, ensure protocol compliance, and contribute to the successful delivery of complex clinical research programmes.

What You'll Be Doing

  • Conducting site qualification, initiation, monitoring, and close-out visits (approximately 6-8 visits per month).
  • Managing investigative sites throughout the full clinical trial lifecycle.
  • Reviewing source data and study documentation to ensure quality, compliance, and patient safety.
  • Supporting site selection and feasibility activities.
  • Training and mentoring site personnel on protocol requirements and GCP standards.
  • Resolving site issues and data queries in collaboration with cross-functional study teams.
  • Maintaining regulatory documentation and supporting audit readiness.
  • Monitoring investigational product accountability and study conduct.
  • Building strong relationships with investigators and site staff to drive study performance.

What We're Looking For

  • Degree in Life Sciences, Pharmacy, Medicine, or a related scientific discipline.
  • Prior experience working as a Clinical Research Associate with independent site monitoring responsibilities.
  • Strong knowledge of ICH-GCP, clinical trial regulations, and site management best practices.
  • Oncology, Haematology or Neurology study experience
  • Ability to work autonomously while collaborating effectively with global study teams.
  • Full-service monitoring experience is advantageous.
  • Fluent German and strong English language skills.
  • Valid driving licence and willingness to travel throughout Germany.

Why Consider This Opportunity?

Home-based flexibility

Exposure to both oncology and neurology studies and opportunity to broaden therapeutic experience

Opportunity to work within a growing international clinical research environment

Strong emphasis on quality, collaboration, and professional development

Meaningful work contributing to the advancement of treatments for patients worldwide

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i‑Pharm Consulting

Kontaktdaten:

i‑Pharm Consulting Recruiting-Team