Remote Jobs at Worldwide Clinical Trials
Find your next remote opportunity · 6 Open Positions
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.
Senior Project Manager - CNS
Project Manager responsible for overall management of clinical trials and cross-functional collaboration. Leading technical and operational project aspects in a remote work setting.
Senior Project Manager – Oncology
Senior Project Manager overseeing clinical trials in Oncology for a global CRO. Ensuring project deliverables and deadlines are met with a focus on quality and operational excellence.
Director, Quality Vendor and Digital Data
Director of Quality Vendor and Digital Data overseeing compliance and quality at Worldwide Clinical Trials. Leading a global team to ensure GxP compliance and drive continuous improvement.
People Systems Administrator, Workday, HRIS
People Systems Administrator for Worldwide Clinical Trials performing Workday administration and providing remote support across global teams.
Senior Regulatory & Site Activation Specialist
Regulatory Affairs Specialist managing and submitting regulatory documents for global CRO. Ensuring compliance with ICH GCP and engaging with local authorities in Australia.
Senior Medical Writer
Senior Medical Writer leading medical writing for Phase I-IV study documents in a global CRO. Collaborating with experts to ensure compliance with regulatory requirements across various regions.
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