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. ...
Strong knowledge of clinical research regulations (ICH-GCP, ISO 14155, FDA, and EU). Having received their series B not too long ago, they are making great strides in the product development for their minimally invasive product and they are looking for a clinical trial manager or senior CRA to aid t...
Job Title: Senior Clinical Research Associate. We are seeking a highly experienced Senior Clinical Research Associate (CRA) to join our dynamic team. The ideal candidate will have a strong background in clinical research, with a focus on monitoring and ensuring the integrity of our clinical trials. ...
Job Title: Senior Clinical Research Associate. Bachelor’s degree in a relevant field or a nursing degree, with 4+ years of experience in clinical research, preferably in a sponsor company, CRA, or CRO setting. Collaborate with the Study Lead and project team to ensure the quality execution of clinic...
We are seeking a Clinical Research Associate I (CRAI) who will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study. The Biomedical Imaging Research Institute (BIRI) is an interdisciplin...
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 works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement stud...
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 ...
As a Clinical Research Associate, you will play a crucial role in the planning, execution, and monitoring of medium and large-sized clinical trials. They are seeking a seasoned Clinical Research Associate to join their growing team. BS/BA in relevant discipline and at least 4 years of industry exper...
The Clinical Research Associate will provide support to the Senior Director, Clinical Operations in managing and tracking key study deliverables and milestones. Minimum 5 years of experience directly supporting oncology clinical research trials in-house at a pharmaceutical company or CRO. This posit...
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 Research Scientist IV (RSIV) (Microbiological Sciences), acting as the Center Biosafety Officer, develops the Center for Laboratory Sciences biosafety, accident prevention and laboratory occupational health programs based on advanced research of infectious disease organism and toxic chemical han...
Under the general direction of the Public Health Medical Administrator I, Division Chief of the Division of Communicable Disease Control (DCDC), the Research Scientist Manager (RSM) serves as the IB Chief within the DCDC. ...
We work hand-in-hand with researchers of the Scripps Research Translational Institute and Calibr to merge foundational studies in biology, chemistry and computer science with translational science to produce pioneering drugs and advances in digital and precision medicine. Scripps Research is a nonpr...
At least 5 years (Research Associate) or 10 years (Senior Research Associate) of experience in analytical development and quality control. ...
This position supports the California Department of Public Health’s (CDPH) mission and strategic plan by performing as a clinical chemistry scientist to ensure the quality of performance and outcomes of results from our highly complex Clinical Laboratory Improvement Amendments (CLIA) certified genet...
The Governor’s Office of Planning & Research (OPR) seeks to fill a Limited-Term/Full-time Associate Governmental Program Analyst (AGPA) position in the Strategic Growth Council, Energy Investments division. Under the guidance of the Solar for All Program Lead, the Solar for All Associate Planner pla...
The Program/Project Coordinator provides strategic support to a mid to large scale, recognized organizational program/project by coordinating all operations for the assigned program or project to facilitate the effective management of programs/projects according to organizational standards. Program ...
We are seeking an experienced Project Manager to oversee the comprehensive execution and daily operations of project design, procurement, and construction. As the client's primary liaison, the Project Manager collaborates directly with the client, project sub-consultants, and subcontractors. Provide...
The Construction Project Coordinator assists in overseeing the development of all assigned projects from inception through project close-out while following practices, policies and guidelines of the capital project development program at CSMC. The Construction Project Coordinator assists the Archite...
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on each study ...
The Program/Project Coordinator in the Heart Institute provides strategic support to a mid to large scale, recognized organizational program/project by coordinating all operations for the assigned program or project to facilitate the effective management of programs/projects according to organizatio...
As a Company Secretarial Assistant, your purpose will be to collaborate with the Company Secretariat team to support Cancer Research UK’s Trustees, CEO, Executive team, General Counsel & Company Secretary in delivering an effective and efficient approach to the charity’s governance. At Cancer Resear...
Acts as responsible for new research, IP, publications, technology roadmap. ...