Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world. 

With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research. 

Make an Impact as a Clinical Research Associate at Worldwide

Bring your oncology and hematology monitoring experience to a role where your work directly supports high-quality clinical research and, ultimately, better outcomes for patients.

As a Clinical Research Associate, you’ll take ownership of site activities throughout the study lifecycle, from qualification and initiation through ongoing monitoring and close-out. You’ll work closely with study sites and colleagues, helping ensure protocol adherence, patient safety, reliable data, and effective site management.

You’ll join a supportive Clinical Operations environment where collaboration is central to how we work. You’ll also have opportunities to share your expertise by mentoring less experienced CRAs and guiding site staff when needed.

Where You'll Work

This is a home-based Clinical Research Associate role supporting sites across Czechia/Slovakia. Candidates must reside within the territory to effectively support site visits and study activities. You will collaborate with sites, sponsors, and global study teams while traveling to investigative sites approximately 8-10 days per month.

To best support our sites, we're seeking candidates who are based in Czechia/Slovakia. Travel will primarily be regional, with occasional travel to support sites in other locations as needed.

What You'll Do

• Manage site qualification, initiation, interim monitoring, site management, and study close-out visits.
• Monitor study sites for protocol adherence, patient safety, data quality, and overall study compliance.
• Review source documentation, informed consent, subject safety information, and CRFs to help ensure accurate and reliable study data.
• Train and support site staff on study protocols and help sites resolve data queries across paper and electronic data capture systems.
• Document site visit findings through clear, accurate, and timely monitoring reports.
• Maintain relevant site documentation for the Trial Master File (TMF) and support effective study documentation management.
• Oversee investigational product receipt, accountability, return, or destruction at study sites.
• Mentor less experienced CRAs and conduct accompanied site visits for assessment or training when required.

What You'll Bring

• A 4-year university degree or RN/BSN in Nursing.
• At least 2 years of experience as a Clinical Research Associate.
• Required experience in both Oncology and Hematology.
• Experience in full-service monitoring required
• Proficiency in English and Czech
• Strong interpersonal, written and verbal communication skills, with excellent organization and attention to detail.
• Ability to work independently with little or no supervision.
• Proficiency in Microsoft Office, CTMS, and EDC systems, together with willingness to travel as required.
   

Discover the Difference

We love knowing that someone is going to have a better life because of the work we do.  Discover the Difference at Worldwide Clinical Trials. Explore additional opportunities on our careers page, visit http://www.worldwide.com/careers, or connect with us on LinkedIn.