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Jobs Send job Detailed job description and main responsibilities Clinical Assist research nurses/ACP's/Clinicians in delivery of patient care to research participants. Support and co-ordinate obtaining and processing of blood and tissue samples in the clinical setting as well as optimising recruitment ...
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Southern Cross University’s National Centre for Naturopathic Medicine is seeking a Clinical Trials Research Fellow to support the Centre by contributing to clinical trial research activities, and support funding applications. This role is integral to advancing the Centre’s mission of evidence-based res...
Serve as back-up medical monitor to provide medical support to trial sites and clinical operation team. Support regulatory filing where medical expertise is required. Support drug discovery when clinical experience is needed for the medical “translation”. ...
Support project leaders in monitoring and tracking the progress of clinical trial deliverables This role requires an experienced research assistant that will have hands-on experience in coordinating and managing clinical trials, providing valuable insight into the research process and contributing to meaningf...
They will also direct the activities of clinical trial staff engaged in clinical research projects to ensure compliance with protocols and overall research objectives. Your key responsibilities will be to: lead the clinical trial operations, and oversee the timely delivery of all clinical trials, ...
research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your ...
李女士/HR 立即沟通 辟埃赛医药科技(上海)有限公司 PSI is a leading full-service global Contract Research Organization providing a wide range of clinical trial services to the pharmaceutical and biotechnology industry, mainly for the ... 公司主页...
1. Support medical director in drafting clinical trial protocol and study report. 2. Contribute to the medical/scientific input given for the development of trial-related documents such as IB, ICF etc. and processes which reside in other line functions. ...