Worldwide Clinical Trials
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 • Rare Disease Clinical Research • Oncology Clinical Research • IMID Clinical Research • Cardiovascular and Metabolic Clinical Research
Senior Clinical Research Associate - CNS
April 15
Worldwide Clinical Trials
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 • Rare Disease Clinical Research • Oncology Clinical Research • IMID Clinical Research • Cardiovascular and Metabolic Clinical Research
📋 Description
• Conduct site qualifications, initiation, interim monitoring, site management and study close-out visits • Review study subject safety information and informed consent • Actively participate in study team and investigator meetings • Compile and ensure completeness of regulatory documents and ethical submission documentation
🎯 Requirements
• At least two years of independent clinical monitoring experience • Demonstrable experience in handling multiple protocols across various therapeutic indications • Excellent interpersonal, oral, and written communication skills in English and local language • Superior organizational skills with attention to detail, and the ability to work independently • Proficiency in Microsoft Office, CTMS, and EDC Systems • Ability to meet the travel requirements of the job
🏖️ Benefits
• Equal employment opportunities for all employees and applicants regardless of various factors • Commitment to attracting diverse talent and cultivating an inclusive environment • Support and professional development to succeed in your role • Emphasis on personalized attention in healthcare
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