About Worldwide Clinical Trials  

Worldwide Clinical Trials is a leading full-service global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new treatments.  

Our capabilities include bioanalytical laboratory services, Phase I-IV clinical trials, and post-approval and real-world evidence studies – all powered by our team members who bring their expertise and a collaborative, personalized approach to each clinical program. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.  
Our talented team of 3,000+ professionals spans 60+ countries, and embraces a culture of diversity, equity, inclusion, and belonging (DEI&B). We are united in cause with our customers to improve the lives of patients through new, innovative therapies.   

For more information on Worldwide, visit www.Worldwide.com.

Biotechnology

Clinical Trials

Worldwide Clinical Trials

Worldwide Clinical Trials' headquarters in Research Triangle Park, NC, United States

The Paris office focuses on regulatory compliance, project management, clinical trials, and risk management in the pharmaceutical sector.

Paris

The Prague office focuses on medical affairs and CNS therapeutic development, driving innovation in healthcare solutions.

Prague

This department functions to analyze and manage statistical data through programming, supporting biostatistics efforts in research and development.

Statistical Programming

The Clinical Research Operations team at Worldwide Clinical Trials is responsible for the design, execution, and management of clinical trials across various therapeutic areas. This team collaborates with cross-functional partners to ensure that studies are conducted efficiently and in compliance with regulatory standards, focusing on patient safety and data integrity. Their expertise enables the seamless coordination of clinical activities, site management, and stakeholder communication, ultimately contributing to the advancement of innovative therapies for patients worldwide.

Clinical Research Operations

The Project Management team at Worldwide Clinical Trials plays a pivotal role in overseeing and coordinating clinical trial activities across various therapeutic areas, including oncology, neurology, and rare diseases. This team is responsible for ensuring that projects are delivered on time, within budget, and in accordance with regulatory guidelines. Through strategic planning and effective communication with stakeholders, they facilitate the successful execution of clinical programs, driving advancements in innovative therapies and enhancing patient outcomes.

Project Management

This department focuses on managing and coordinating the processes involved in the activation of clinical trial sites to ensure efficient operations and compliance with regulatory standards.

Site Activation

This department manages compliance and regulatory processes to ensure products meet legal standards and industry regulations.

Regulatory Affairs

This department manages the operations related to Trial Master Files (TMF), ensuring compliance and quality throughout the lifecycle of clinical trials.

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Other teams

Clinical Research Operations

Project Management

Site Activation

Regulatory Affairs

TMF Operations