
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.
2 days ago

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.
• Prepare and lead the medical writing team on Phase I-IV study documents such as protocols and protocol amendments • Work with other departments in Worldwide preparing and leading the development of Pre-IND documents • Responsible for key documents template management in accordance with global regulations
• University/college degree (life science or related allied health profession) or equivalent combination of education and experience • Minimum of 4 years of experience as a Medical Writer or equivalent role • Excellent written and spoken English • Ability to accurately interpret data
• Ongoing training and career development opportunities • Diverse and inclusive work environment • Accessible leadership
Apply NowNovember 25
1001 - 5000
Medical Writer preparing clinical evaluation plans and reports for global medtech company. Collaborating with teams on clinical evaluation strategies and conducting literature reviews.
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⏰ Full Time
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