
1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.
🕒 May 15
Where this job comes from
Posted on Worldwide Clinical Trials's careers page, not through a job board
First seen by Remote Rocketship May 15

1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.
• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects • Conduct study initiation visits (SIVs) • Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements
• 5+ years of experience as a Clinical Research Associate • 4-year university degree OR Nursing Degree • Experience in Oncology and Rare Disease is required • Fluent in written and verbal English required • Candidates must reside in Brazil • Willingness to travel regionally required
• Health insurance • Paid time off • Flexible working arrangements • Professional development opportunities
Apply NowImprove your chances of getting an interview by checking your resume score before you apply.
🕒 February 20
Lead Data Manager responsible for all data management activities in clinical trials. Overseeing data collection, validation, and ensuring data quality in clinical projects.