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Worldwide Clinical Trials Holdings is a global, midsize Contract Research Organization (CRO) dedicated to innovating and advancing clinical research to improve patient lives. With a team of over 3,500 experts, the company fosters a culture of collaboration, creativity, and inclusivity, ensuring that every employee plays a vital role in making a difference for patients and caregivers. Committed to quality and excellence, Worldwide Clinical Trials emphasizes professional development and offers clear career paths within a supportive environment. The organization specializes in various therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases, and is driven by a mission to provide personalized attention and exceptional employee experiences.
W.C.T
Worldwide Clinical Trials
Join Worldwide Clinical Trials as a Senior Project Manager to lead and manage clinical trials in the Oncology therapeutic area.
W.C.T
Worldwide Clinical Trials
The Medical Director in Medical Affairs is responsible for overseeing clinical investigations and collaborating with various teams to enhance patient outcomes.
W.C.T
Worldwide Clinical Trials
Join Worldwide Clinical Trials as a Senior Regulatory Affairs Specialist, supporting regulatory submissions and site activation for clinical trials across the EU.
W.C.T
Worldwide Clinical Trials
The Director of Project Management will lead large-scale clinical projects focused on Obesity/GLP1, ensuring high-quality outcomes and effective team collaboration.
W.C.T
Worldwide Clinical Trials
Join Worldwide Clinical Trials as a Senior Clinical Research Associate to manage clinical research activities remotely and ensure compliance with regulatory standards.
W.C.T
Worldwide Clinical Trials
Join Worldwide Clinical Trials as a Senior Clinical Research Associate, managing remote research activities in metabolic and obesity studies.
W.C.T
Worldwide Clinical Trials
Join Worldwide Clinical Trials as a Senior Director of Data Management Operations, leading a global team to ensure high-quality data management in clinical studies.
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