Remote CRA II: Oncology/Neurology — Germany

Worldwide Clinical Trials; United States; Remote; USD 79,000 - 112,000; Full time

Job summary

Worldwide Clinical Trials is seeking a CRA II for a home-based position supporting sites in Germany. You will monitor trials, ensure data integrity, and maintain regulatory compliance across study life-cycle from activation to close-out.

Expect collaboration with study teams, sponsors, and investigative sites, with approximately 6–8 site visits monthly. Fluency in German and strong English are required.

Qualifications

• MD/DO/PharmD or life sciences degree with clinical research experience.
• Minimum CRA II level experience in clinical research and monitoring.
• Thorough understanding of GCP, ICH, FDA/EU regulations, and local rules.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits per protocol and regs.
• Evaluate site feasibility and support site selection for studies.
• Review source documentation and data to ensure accuracy, safety, protocol adherence, and data integrity.
• Prepare and verify regulatory and ethics documentation for study conduct.
• Train and support site personnel on protocol requirements and GCP.

Skills

CRA II experience

Site monitoring

GCP knowledge

English proficiency

Education

Life sciences degree

Tools

MS Office

EDC systems

IxRS

Job description

Worldwide Clinical Trials is seeking a CRA II for a home-based position supporting sites in Germany. You will monitor trials, ensure data integrity, and maintain regulatory compliance across study life-cycle from activation to close-out.

Expect collaboration with study teams, sponsors, and investigative sites, with approximately 6–8 site visits monthly. Fluency in German and strong English are required.