About this role
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 Trial Associate at Worldwide
As a Senior Clinical Trial Associate, you will play a key role in supporting the successful delivery of clinical studies by ensuring essential project activities are completed accurately, efficiently, and on time. Your work will help clinical teams stay organized, compliant, and focused on advancing research that can ultimately improve patient outcomes.
Working closely with Project Managers, CRAs, and cross-functional study teams, you will provide critical administrative, documentation, and project tracking support across multiple clinical projects. You'll also contribute to process improvements, support team development, and help drive quality throughout the study lifecycle.
Where You'll Work
This is a REMOTE role open to candidates based in Taiwan. You will collaborate with global teams across multiple time zones.
What You'll Do
- Coordinate and track project team system access to ensure teams can effectively support study delivery.
- Maintain project portals and perform quality checks to ensure documentation is current, accurate, and accessible.
- Support the preparation, management, and shipment of clinical trial documentation, including Investigator Site Files.
- Manage version control and quality review of project documents and ensure timely submission to the Trial Master File.
- Track and maintain key project information, including site communications and medical question logs.
- Prepare and distribute meeting minutes for sponsor, project, and internal management meetings.
- Maintain accurate site and study personnel records to support efficient study operations.
- Coordinate project-specific training activities and monitor completion across study teams.
- Contribute to onboarding, coaching, training, and leadership of Clinical Trial Associates while supporting continuous process improvement initiatives.
What You'll Bring
- Degree-level qualification or equivalent experience, plus a minimum of two years of experience in a related role.
- Proficiency in English and fluency in the local language of the country of location.
- Strong interpersonal skills with the ability to collaborate effectively across project teams.
- Ability to work independently with minimal supervision while contributing as a team member.
- Strong organizational, problem-solving, and multitasking skills in a fast-paced environment.
- Excellent attention to detail and commitment to quality.
- Ability to mentor, coach, and support the development of colleagues.
- Working knowledge of ICH, GCP, and applicable FDA or EU regulatory requirements, along with strong proficiency in Microsoft Outlook, Word, Excel, and PowerPoint.
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.