Worldwide Clinical Trials
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
Senior Clinical Research Associate – Oncology, CNS
November 21
Worldwide Clinical Trials
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
📋 Description
• Conduct all types of visits – site qualifications, initiation, interim monitoring, site management and study close-out visits • Review study subject safety information and informed consent and conduct source document verification for compliance, patient safety, and veracity of data • Actively participate in study team and investigator meetings • Compile and ensure completeness of regulatory documents and ethical submission documentation and review study subject safety information and informed consent and study material (e.g. CRFs, manuals)
🎯 Requirements
• At least two years of independent clinical monitoring experience • Demonstrable experience in handling multiple protocols across a range of therapeutic indications • Four-year college curriculum in life sciences, OR • Two-year college curriculum or equivalent education/training (nursing degree or equivalent life science degree) • Ability to meet the travel requirements of the job • 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 • Broad understanding of clinical research principles and process • Proficiency in Microsoft Office, CTMS, and EDC Systems
🏖️ Benefits
• Accessible leadership team • Cohesive and supportive teams • Diversity and inclusion initiatives • Professional development support • Career path guidance to Clinical Trial Manager roles
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