Senior Clinical Research Associate - SK

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 Senior Clinical Research Associate at Worldwide

Play a key role in advancing clinical research by ensuring studies are conducted with the highest standards of quality, compliance, and patient safety. As a Senior Clinical Research Associate, you'll serve as a trusted partner to investigative sites, sponsors, and study teams, helping drive the successful execution of clinical trials that support the development of new therapies.

In this role, you'll take ownership of site monitoring activities, build strong relationships with investigators and site staff, and provide expert oversight throughout the study lifecycle. Your contributions will help ensure data integrity, regulatory compliance, and timely study delivery.

Working closely with global and cross-functional teams, you'll have the opportunity to make a meaningful impact on study outcomes while supporting the advancement of innovative treatments for patients worldwide.

Where You'll Work

This is a home-based Clinical Research Associate role supporting sites across South Korea. 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 South Korea. Travel will primarily be regional, with occasional travel to support sites in other locations as needed.

What You'll Do

• Monitor clinical trial sites to ensure compliance with study protocols, regulatory requirements, GCP, and sponsor expectations.
• Build and maintain strong partnerships with investigators and site personnel to support successful study execution.
• Oversee site performance, data quality, patient safety, and study documentation throughout the clinical trial lifecycle.
• Identify, investigate, and proactively resolve site-related issues that may impact study quality, timelines, or compliance.
• Collaborate with sponsors and cross-functional teams to drive study progress and achieve key milestones.
• Conduct site visits, provide training and guidance to site staff, and support inspection readiness activities.
• Maintain accurate monitoring documentation and communicate study updates, risks, and recommendations to stakeholders.
• Contribute to continuous improvement initiatives that enhance study execution, monitoring effectiveness, and operational quality.

What You'll Bring

• Degree-level education or an equivalent qualification, combined with relevant clinical research experience in monitoring and managing clinical trial sites.
• Strong understanding of ICH-GCP, regulatory requirements, and clinical trial processes.
• Demonstrated ability to independently manage multiple sites, priorities, and study activities while maintaining quality and timelines.
• Experience collaborating with investigators, site personnel, sponsors, and cross-functional study teams.
• Excellent analytical, problem-solving, organizational, and communication skills with strong attention to detail.
• Ability to identify risks, drive issue resolution, and support inspection-ready study conduct.
• Experience in full-service monitoring PREFERRED.
• Proficiency in English.

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.