Clinical Research Associate

Established Search; Düsseldorf; Remote; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A leading clinical research organization seeks a Clinical Research Associate (CRA) to monitor clinical trial sites mainly in Eastern Germany. The ideal candidate will have at least 5 years of experience in Pharma-sponsored Oncology trials and strong communication skills in both German and English. The remote position offers flexibility and the chance to work on impactful clinical programs with leading pharmaceutical companies.

Leistungen

Flexibility and autonomy

Supportive, science-driven culture

Qualifikationen

• Minimum 5 years of CRA experience, preferably in Pharma-sponsored trials.
• Experience in Oncology trials is a must; knowledge of IVD studies is a plus.
• Deep understanding of GCP, ICH, and German regulations.

Aufgaben

• Monitor clinical trial sites for compliance with protocols and regulations.
• Conduct routine monitoring visits including site initiation and close-out.
• Perform source data verification and maintain accurate documentation.
• Support study start-up activities like EC/IRB submissions.

Kenntnisse

Fluent German

Professional English

Monitoring clinical trial sites

GCP understanding

Organizational skills

Communication skills

Problem-solving skills

Jobbeschreibung

Role : Clinical Research Associate (CRA)

Location : Remote, based in Eastern Germany

Languages : Fluent German and professional English required

About the Company

Our client is a well-established European Contract Research Organization (CRO) known for delivering high-quality, full-service clinical trial solutions across multiple therapeutic areas. With a strong reputation for operational excellence, sponsor collaboration, and scientific rigor, the organization partners with top-tier pharmaceutical companies and biotech firms to bring innovative therapies to patients efficiently.

They offer a supportive, science-driven culture with flexibility and autonomy, ensuring each team member plays a key role in high-impact clinical programs.

The Role

The Clinical Research Associate (CRA) will be responsible for monitoring clinical trial sites, primarily in Eastern Germany, to ensure compliance with protocols, GCP, and regulatory requirements. This role is remote-based and ideal for an experienced CRA with a strong background in Oncology trials and Pharma sponsor collaborations. Experience with IVD studies is highly desirable.

Key Responsibilities

• Conduct routine monitoring visits including site initiation, interim, and close-out visits.
• Ensure compliance with ICH-GCP, German regulations, and study-specific protocols.
• Perform source data verification and ensure accurate documentation in the eTMF.
• Build and maintain effective relationships with site staff, investigators, and sponsors.
• Identify and address site performance or compliance issues proactively.
• Support study start-up activities, including EC / IRB submissions and site feasibility assessments.
• Collaborate with project management, data management, and medical teams to ensure timely and quality trial delivery.

Requirements

• Minimum 5 years of CRA experience, with significant exposure to Pharma-sponsored trials.
• Proven experience in Oncology trials; additional therapeutic areas are a plus.
• Experience with IVD studies is desirable.
• Deep understanding of GCP, ICH, and German regulatory requirements.
• Fluent in German (native or near-native) and professional English.
• Ability to travel across Germany as required.
• Strong organizational, communication, and problem-solving skills.
• Self-motivated, proactive, and comfortable working remotely.

Why Apply

• Join a highly respected European CRO delivering cutting-edge clinical research.
• Work in a remote-based role with flexibility and autonomy.
• Engage in Oncology-focused, high-impact clinical trials in collaboration with leading Pharma sponsors.