CRA (multiple levels)

Barrington James; Stuttgart; Hybrid; EUR 40.000 - 60.000; Vollzeit

Zusammenfassung

A global leader in clinical research is hiring Clinical Research Associates at multiple levels to support a diverse portfolio of international clinical trials in Germany. This role can be performed remotely or in-office, offering opportunities for professionals ranging from entry-level to whom can mentor others. Responsibilities involve ensuring protocol adherence and maintaining data integrity while providing essential support for clinical studies. Ideal candidates will possess a strong commitment to collaboration and quality, along with relevant educational backgrounds in life sciences or related fields.

Qualifikationen

• Bachelor’s degree in a life sciences, nursing, pharmacy, or healthcare-related field is mandatory.
• Fluency in both German and English is required.
• Strong commitment to quality, compliance, and collaboration is essential.

Aufgaben

• 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.

Kenntnisse

Organisational skills

Fluency in German

Fluency in English

Compliance commitment

Collaboration

Ausbildung

Bachelor’s degree in life sciences

Nursing degree

Pharmacy degree

Healthcare-related degree

Jobbeschreibung

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 (1–2 years of experience)

• 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