
1001 - 5000 employees
đ§Ź Biotechnology
đ Pharmaceuticals
âď¸ Healthcare Insurance
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.
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1001 - 5000 employees
đ§Ź Biotechnology
đ Pharmaceuticals
âď¸ Healthcare Insurance
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.
⢠Responsible for the full life cycle of sponsor contracts/change orders ⢠Responsible for preparing the contract by drafting and/or incorporating the associated budget, scope of work, and legal, financial, and operational terms ⢠Collaborate with Business Development, Therapeutic Leaders, Operations, Finance and Legal departments to draft and finalize contracts/change orders ⢠Lead and participate in conference calls to negotiate terms of an agreement, including the study budget, with the sponsor ⢠Develop and/or modify service description text in addition to original proposal text, which collectively becomes the core contract/exhibit ⢠Liaise with Project Management Lead and other functional departments in order to finalize timelines, project scope and associated costs
⢠Bachelor's degree or equivalent work experience ⢠Two to three years of direct experience with CRO or pharmaceutical data; sourcing, integration, analysis, and reporting ⢠Advanced Proficiency in MS Office
⢠Inclusive workplace where professionals from all backgrounds thrive ⢠Professional development opportunities
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