Clinical Research Associate

Barrington James; Düsseldorf; Remote; EUR 45.000 - 80.000; Vollzeit

Zusammenfassung

A leading company in the clinical research field is hiring Clinical Research Associates in Germany, offering roles from entry-level to senior positions. The job involves managing clinical trials, ensuring compliance, and collaborating with study site teams. This flexible role provides opportunities to work remotely or from the office, catering to various experience levels in a challenging and rewarding environment.

Qualifikationen

• Exposure to site monitoring or clinical operations is desired for CRA I.
• Track record in managing monitoring visits expected for CRA II.
• Leadership and mentoring capabilities required for Senior CRA.

Aufgaben

• Conduct site qualification, initiation, and monitoring visits.
• Ensure compliance with ICH-GCP and protocol requirements.
• Liaise with investigators for smooth trial conduct.

Kenntnisse

Organisational Skills

Fluency in German

Fluency in English

Commitment to Quality

Collaboration

Ausbildung

Bachelor’s degree in a life sciences, nursing, pharmacy, or healthcare-related field

Jobbeschreibung

• YOU MUST BE BASED IN GERMANY AND HAVE PREVIOUS CRA EXPERIENCE TO APPLY

Clinical Research Associate – Germany (Remote or Office-Based)

CRA (Entry-Level to Senior CRA) – Multiple Openings

We’re hiring Clinical Research Associates at three levels to support a portfolio of international clinical trials. These are permanent roles based in Germany, with the flexibility to work fully remote or from an office.

If you’re early in your CRA career or bring years of site monitoring expertise, we’d love to hear from you.

About the Role

You’ll play a central part in the execution of clinical studies, supporting patient safety, protocol adherence, and data integrity across a variety of therapeutic areas.

Key Responsibilities

• Conducting site qualification, initiation, routine monitoring, and close-out visits
• Ensuring compliance with ICH-GCP, protocol requirements, and local regulations
• Liaising with investigators and study site teams to ensure smooth trial conduct
• Performing source data verification, addressing queries, and maintaining quality standards
• Supporting the review of clinical study documentation (protocols, reports, etc.)

Levels & Experience

CRA I (0–2 years of experience)

• Ideally some exposure to site monitoring or clinical operations (e.g. CTA or junior CRA background)
• Strong organisational skills and willingness to learn in a fast-paced environment

CRA II (2–5 years of experience)

• Proven track record of independently managing monitoring visits
• Strong knowledge of GCP, clinical trial processes, and regulatory requirements

Senior CRA (5+ years of experience)

• Confident leading site relationships and supporting trial planning activities
• May support training or mentoring of junior CRAs

Core Requirements for All Levels

• Bachelor’s degree in a life sciences, nursing, pharmacy, or healthcare-related field
• Fluency in German and English
• Willingness to travel for on-site visits
• A strong commitment to quality, compliance, and collaboration