Clinical Research Associate | Germany | Remote-Grade 11

📍 Wiesbaden, Germany (Remote Eligible)
🕒 Full-Time | AbbVie | Global Grade 11

Job Overview

AbbVie is hiring a Clinical Research Associate (CRA) to support the planning, monitoring, and execution of Phase I–IV clinical trials. This full-time role is remote-friendly for professionals based in Wiesbaden, Germany, and focuses on ensuring compliance with ICH-GCP guidelines, local regulations, and AbbVie SOPs while maintaining the highest standards of data quality and patient safety.

This is an excellent opportunity to grow your career with a global biopharmaceutical leader working across immunology, oncology, neuroscience, and eye care.

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Key Responsibilities

• Manage and monitor clinical trial sites across multiple protocols and therapeutic areas

• Ensure clinical trials are conducted in accordance with GCP, ICH guidelines, EU regulations, and AbbVie SOPs

• Support study startup, site initiation, interim monitoring, remote monitoring, and study closeout activities

• Ensure accurate, timely, and compliant data collection and safety reporting

• Protect the rights, safety, and well-being of clinical trial participants

• Train investigators and site staff on study protocols and regulatory requirements

• Conduct or support site qualification, initiation, monitoring, and closeout visits

• Prepare and submit monitoring visit reports and regulatory documentation

• Support Clinical Trial Applications (CTA), informed consent updates, and local language translations

• Assist with study budgets, clinical trial agreements, and investigator payments

• Ensure audit and inspection readiness at assigned sites

• Escalate risks, deviations, and quality issues appropriately

• Support innovative tools and processes to improve clinical operations efficiency

Required Qualifications

• Degree or equivalent experience in life sciences, healthcare, or a related field

• 1+ year of experience in clinical research, pharmaceutical, or healthcare settings (preferred)

• Experience with industry-sponsored clinical trials (CRA, CTA, Study Coordinator, Data Manager, or similar) preferred

• Strong knowledge of ICH-GCP guidelines and EU clinical trial regulations

• Excellent organizational, analytical, and communication skills

• Ability to manage multiple studies and competing deadlines

• High standards of professional ethics and integrity

What AbbVie Offers

• Competitive salary and benefits package

• Remote and flexible working models (Germany-based)

• Structured onboarding program with a dedicated mentor

• Comprehensive corporate health and wellness programs

• Long-term career development and international mobility opportunities

• Inclusive, diverse, and collaborative global work culture

This role is ideal for professionals located in Wiesbaden, Frankfurt, Mainz, Darmstadt, and the greater Hesse (Hessen) region, with flexibility to work remotely while supporting clinical trial sites across Germany and Europe.

Related: Senior Patient Access Specialist

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