CRA II / Senior CRA - remote working

i‑Pharm Consulting; Deutschland; Remote; EUR 60.000 - 85.000; Vollzeit

Zusammenfassung

i‑Pharm Consulting is partnering with a global CRO to hire a CRA II/Senior CRA to support oncology and neurology studies across Germany. You will manage site relationships, ensure protocol compliance, and contribute to complex clinical programmes from a home-based setup.

The role requires experience as a CRA with independent monitoring, strong ICH-GCP knowledge, and fluency in German and English. Travel across Germany is expected, with opportunities for professional development within a

Qualifikationen

• Degree in Life Sciences, Pharmacy, Medicine, or related field.
• Experience as a Clinical Research Associate with independent site monitoring.
• Strong knowledge of ICH-GCP and site management.
• Oncology, Haematology or Neurology study experience.
• Fluent German and strong English.
• Valid driving licence and willingness to travel across Germany.

Aufgaben

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

Kenntnisse

German (Fluent)

English (Strong)

Autonomy

Willingness to travel

ICH-GCP knowledge

Ausbildung

Life Sciences/Pharmacy/Medicine degree

Jobbeschreibung

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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