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...
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. The Cancer Center Protocol Office is seeking motivated, detail-oriented individuals ...
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...
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...
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...
Clinical Research Associate will oversee outsourced clinical operations activities including but not limited to site management, site monitoring and site level TMF filing. A minimum of 7-10 years of experience as a Clinical Research Associate, with at least 2 years in a senior or lead CRA role. In-d...
Job Description - Clinical Research Associate II---Cancer Center Protocol Office (3293250). 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 ...
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). ...
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...
The Clinical Research Associate/Clinical Research Coordinator I (CRA/CRC I) works under general supervision to enroll eligible patients to clinical research protocols and manage all aspects of data collection and submission for multiple cancer studies. The Cancer Center Protocol Office is seeking a ...
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 ...
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...
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...
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...
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. ...
Requires a minimum of three (3) years as CRA experience in the pharmaceutical/biotechnology industries, or with a Clinical Research Organizations (CROs). Clinical Operations team on a contract basis. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines . ...
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-(3301500). The Cancer Ce...
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 ...
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). ...
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...
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 ...