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.
Neuroscience/Central Nervous System Clinical Research β’ Rare Disease Clinical Research β’ Oncology Clinical Research β’ IMID Clinical Research β’ Cardiovascular and Metabolic Clinical Research
6 days ago
π² North Carolina β Remote
β° Full Time
π‘ Mid-level
π Senior
π·ββοΈ Project Manager
π¦ H1B Visa Sponsor
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.
Neuroscience/Central Nervous System Clinical Research β’ Rare Disease Clinical Research β’ Oncology Clinical Research β’ IMID Clinical Research β’ Cardiovascular and Metabolic Clinical Research
β’ Project Manager responsible for overall coordination and management of clinical trials from start-up through closeout activities β’ Directs technical, financial and operational aspects to secure successful completion of clinical trials β’ Works with functional area leads to identify and evaluate fundamental issues and ensure deliverables meet customer expectations
β’ 5 years' industry experience with previous experience in a Clinical Project Management role, within a CRO setting β’ University/College degree, within Life Science is preferred β’ Ability to manage projects in a multi-office environment β’ Excellent interpersonal, oral, and written communication skills in English β’ Superior planning and organizational skills with attention to details β’ Proficiency in Microsoft Office, CTMS and EDC Systems
β’ Equal opportunity employer β’ Committed to enabling professionals from all backgrounds and experiences to succeed β’ Equal employment opportunities to all employees
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