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...
The R&D IS BP, provides single point of contact for designated R&D business functions, and specifically serves as the strategic partner and trusted advisor to assigned Research & Non-Clinical Development (RNCD) functions. Jazz Pharmaceuticals' Information Services (IS) department is seeking an Assoc...
A company is looking for a Clinical Research Associate II. ...
Perform tissue culture work with human cell lines to develop and optimize workflows for cell model creation and quality control.Support project management efforts in standard operating procedure creation, sharing knowledge and skills, and fostering cross-functional teamwork.Work with human cell line...
A company is looking for a Clinical Research Associate in Oncology. ...
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 ...
A company is looking for a Senior Clinical Research Associate. Key Responsibilities:Conduct site monitoring visits in accordance with regulatory requirementsManage progress of assigned studies by tracking regulatory submissions and approvalsCreate and maintain documentation regarding site management...
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...
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 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 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...
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...
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 ...
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 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 ...
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. ...
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 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...
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 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 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...