PhAST is seeking a talented and driven contract laboratory Research Associate with expertise in Clinical Microbiology to execute the experimental program foundational for our diagnostic technology and to move forward our on-going FDA clinical trial. Opening for Contract Research Associate in Clinica...
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...
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 Accelerated Program of Education, Exposure, and Experience for Clinical Research Associates (APEX CRA) provides foundational clinical research trainingincluding project and system experience. Do you have up to 2 years of experience working as a Clinical Research Coordinator in Ophthalmology, Vac...
The Early Clinical Development Senior Clinical Research Associate will have relevant Phase I experience, responsible for conducting monitoring activities for one or more client sponsored studies. CRA functions as a member of the clinical study team and performs study monitoring according to Good Cli...
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 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...
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. ...
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-(3291035). The Cancer Ce...
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. ...
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...
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...
As the Senior Clinical Research Associate (CRA) you will be a key player in managing clinical trials from start to finish, ensuring that projects are executed efficiently, within budget, and in compliance with regulatory guidelines. Bachelor’s degree in Life Sciences, Clinical Research, or a related...
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...
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...
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...
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). ...
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...
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...