Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in c...
The Associate Medical Director will contribute to the direction, planning, execution, and medical oversight of clinical trials and aligned research activities for one or more clinical development programs. Associate Medical Director, Clinical Research. The Clinical development department is responsi...
Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in c...
The Human-centered AI team in Digital Health Oncology R&D is looking for an Associate Director of Data Science to specialize in the development of novel digital endpoints using data science, statistical learning, and innovative machine learning methods on multi-modal datasets including clinical ...
Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in c...
Senior Clinical Research Associate positions open for a Biotechnology client. The ideal CRA will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating p...
Clinical Research Associate II---Cancer Center Protocol Office-(3293250). PCORP is seeking Clinical Research Associate (CRA) candidates to assist with the coordination and monitoring of multiple oncology trials. The Program for the Coordination and Oversight of Research Protocols (PCORP) within the ...
The Clinical Research Associate I (CRA I) works under general supervision to enroll eligible patients to clinical research protocols and manage data collection and regulatory submissions for multiple cancer studies. Clinical Research Associate---Cancer Center Protocol Office-(3301500). The Cancer Ce...
Reporting to the manager of clinical research associates, the person in this role is responsible for the management of day-to- day aspects of investigational site activities on assigned clinical trials. Conduct site monitoring visits and follow-up to identify significant problems and issues and to e...
The Multi-Center Clinical Research Associate/Monitor III (CRA III) works independently, under minimal supervision, to initiate, manage and navigate a portfolio of Investigator-initiated, multi-center clinical research trials. Clinical Research Associate III--Cancer Center Protocol Office-(3292745). ...
The candidate will also manage a team of clinical research coordinators/research assistants to ensure efficient functioning of the clinical and translational research infrastructure. The candidate will report directly to the Director of the Gastrointestinal Cancer Center Program and will be responsi...
Clinical Research Associate II---Cancer Center Protocol Office-(3293250). PCORP is seeking Clinical Research Associate (CRA) candidates to assist with the coordination and monitoring of multiple oncology trials. The Program for the Coordination and Oversight of Research Protocols (PCORP) within the ...
The Associate Medical Director will contribute to the direction, planning, execution, and medical oversight of clinical trials and aligned research activities for one or more clinical development programs. The Clinical development department is responsible for the medical aspects of development acti...
Oversee investigator-initiated and grant funded clinical trials including development of protocols/budgets, support the contract process, and coordinate correlative sample processing Lead process improvement projects to increase accrual and study approval/activation timelines Lead process improvemen...
Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address concerns associated with study delivery at sites within established protocols and portfolio under gene...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
Clinical Research Associate-(3292572). The Clinical Research Associate (CRA) will assist with our study on Mindful Self-Compassion as a treatment for PTSD. Working knowledge of clinical research protocols . As a not-for-profit organization, Mass General Brigham is committed to supporting patient car...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development as a Clinical Research Associate II. ICON plc is a world-leading healthcare intelligence and clinical research organization. Cond...
Senior Clinical Research Associate positions open for a Biotechnology client. The ideal CRA will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating p...
We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development as a Clinical Research Associate II assigned to Early Development trials (Phase I). ICON plc is a world-leading healthcare intell...
As a Clinical Research Associate you will serve as the pivotal link between clinical studies and robust clinical data. Responsibilities Identify, evaluate, and lead the implementation and coordination of clinical studies Serve as the point of contact for study participants throughout IVD medical dev...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
Clinical Research Associate III. We are seeking Clinical Research Associates (CRA) to assist in bringing our device to market. Bs in related scientific field and 3 years of clinical research experience in medical device clinical trials. Establishment and updating the study files, including managing ...
Includes Clinical roles focused on research projects. Positions in this family perform basic, translational, and/or clinical research towards solving a specific problem for an entity or community. This role focuses on performing work related to research and development of new products, innovation, a...