Remote Senior CRA – Czechia | Global Trials

Worldwide Clinical Trials; United States; Remote; USD 46,000 - 62,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate for a home-based role covering sites in Czechia. You will monitor study progress, ensure protocol adherence and regulatory compliance, and support site teams across the trial lifecycle to deliver high-quality data.

You will travel 6–8 days per month, collaborate with investigators, sponsors and global teams, and play a key part in site qualification, initiation, monitoring and closeout activities, while ensuring patient

Qualifications

• 5+ years of regional, traveling Clinical Research Associate experience.
• Willingness to travel within the region; 6–8 days per month.
• Experience in full-service monitoring preferred.
• Strong knowledge of clinical trial processes and regulatory requirements.

Responsibilities

• Manage clinical research activities at investigative sites participating in Worldwide clinical studies.
• Identify and assess potential research sites to support successful study execution.
• Coordinate study start-up activities, including collection of regulatory documentation and support of contract and budget processes.
• Conduct all types of monitoring visits: PSSVs, SIVs, IMVs and COVs.
• Train site personnel on protocol requirements, data collection processes, and safety reporting expectations.
• Monitor site performance and provide ongoing support throughout study maintenance activities.
• Ensure compliance with informed consent requirements, safety reporting obligations, and applicable regulatory standards.
• Partner with sites and study teams to drive data quality, participant safety, and overall study success.

Skills

Travel extensively

Site monitoring

Clinical trial processes

Regulatory compliance

Cross-functional collaboration

Education

Bachelor’s Degree

Nursing Degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate for a home-based role covering sites in Czechia. You will monitor study progress, ensure protocol adherence and regulatory compliance, and support site teams across the trial lifecycle to deliver high-quality data.

You will travel 6–8 days per month, collaborate with investigators, sponsors and global teams, and play a key part in site qualification, initiation, monitoring and closeout activities, while ensuring patient