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. Job Description - Clinical Research Associate III--Cancer Center Protocol ...
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...
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. Bachelors degree in Life Sciences, Clinical Research, or a related ...
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). ...
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. The Cancer Center Protocol Office is seeking motivated, detail-oriented individuals ...
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 . ...
Experienced Clinical Research Associates- a. We are rapidly growing and are seeking experienced Clinical Research Associates to join our team!. Candidates must have at minimum a Bachelors degree in a health or science related field, minimum one year of clinical research experience or relevant direct...
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 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...
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 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...
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...
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...
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 Cancer Center Protocol Office is a centralized clinical research office that supports clinical researchers in all disciplines within the Cancer Center. The Associate Manager provides first-line supervision to research staff members and oversees the day-to-day operations of the staff while mainta...
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...
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). ...
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 MGH Cancer Center Protocol Office specializes in the central coordination,...
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 ...
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. ...
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...