Remote Jobs at Worldwide Clinical Trials

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Worldwide Clinical Trials

Research Services

As a leading full-service global CRO, we work to create solutions that advance new treatments from discovery to reality.

BiotechnologyPharmaceuticalsHealthcare Insurance

Worldwide Clinical Trials (Worldwide) is a full-service global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Worldwide’s capabilities include bioanalytical laboratory services, Phase I-IV clinical trials, and post-approval and real-world evidence studies – all powered by an accessible team of clinicians, scientists, and researchers who bring first-hand expertise and a collaborative, personalized approach to each clinical program. Worldwide is therapeutically focused on neuroscience, oncology, rare disease, cardiometabolic, and immune-mediated inflammatory diseases. Its global footprint spans over 60 countries with more than 3,500 team members. For more information on Worldwide, visit www.worldwide.com.

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4d

Regulatory Affairs Specialist, Remote

Worldwide Clinical Trials

Worldwide Clinical Trials seeks a Regulatory Affairs Specialist in Denmark (remote). Manages submissions, regulatory strategies, and compliance across EU/UK.

🇩🇰 Denmark
Full-time
Mid Level
Senior
🚔 Compliance
Google Cloud Platform
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4d

Senior Clinical Research Associate, Rare/CNS, Southeast, Remote

Worldwide Clinical Trials

Senior Clinical Research Associate for Rare/CNS; Worldwide Clinical Trials, a global CRO, supports site management and regulatory activities remotely in the Southeast.

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13d

Senior Regulatory Affairs Manager, APAC

Worldwide Clinical Trials

Drive regulatory affairs for diverse clinical trials across APAC at Worldwide. Lead submissions, provide expert advice, and mentor junior staff.

Google Cloud Platform
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13d

Financial Systems Analyst

Worldwide Clinical Trials

Financial Systems Analyst troubleshooting requests and ensuring timely resolution at Worldwide Clinical Trials.