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
April 14
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’ Managing research activities at sites for clinical research projects β’ Involved in all stages of clinical study β’ Conducting study initiation visits (SIVs) β’ Ensure compliance with obtaining informed consent and regulatory requirements
β’ 5+ years of experience as a Clinical Research Associate β’ 4-year university degree or RN/BSN in Nursing β’ Experience in Liver Disease is required β’ Excellent interpersonal, oral, and written communication skills in English β’ Superior organizational skills with attention to details β’ Ability to work with little or no supervision β’ Proficiency in Microsoft Office, CTMS and EDC Systems
β’ Accessible leaders β’ Supportive teams β’ Diverse and inclusive environment β’ Career path development β’ Opportunities to advance in clinical research
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