At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success. As a CRA, Parexel will offer you world class technology and trainin...
May be responsible for CRA and CTAs as direct reports. ...
Through questioning the status quo and collaborating cross-functionally, the Manager, Clinical Operations provides leadership to a team of Clinical Research Associates (CRAs) and ensures the successful performance and delivery of his/her direct report’s project deliverables, on time with high qualit...
At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success. As a CRA, Parexel will offer you world class technology and trainin...
We are looking for an experienced Clinical Research Associates (CRAs) to add to our dynamic research team. Assist Clinical Research Coordinators (CRC) with Electronic Data Capture (EDC) and resolving Queries using Sponsor database. Assist Clinical Research Coordinators (CRC) with quality assurance (...
Senior Research Associate II, Analytical Operations. Excellent employment opportunity for a Senior Research Associate at Gilead, Oceanside, CA. ...
Join out amazingly talented research and bet at the forefront of our active clinical trials. The ideal applicant is a pre-med student, foreign medical graduate, or medical assistant with a true inquisitive passion. Working knowledge of clinical research policies and guidelines set forth by: US - Foo...
Clinical Operations plays a key role in ensuring all Client clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of Client products. Clinic...
The Clinical Trial Associate will assist and work in collaboration with the Program(s) Lead/Manager of Clinical Operations (or another member of the departmental leadership team), to ensure timely completion of program activities. Coordinate the development of Clinical Trial Agreements with appropri...
The Clinical Research Associate II works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse, or Principal Investigator to coordinate and/or implement the study and may serve as the point of contact for the external sponsors. Works with a Clinical Researc...
Align yourself with an organization that has a reputation for excellence! Cedars-Sinai received the National Research Corporation’s Consumer Choice Award 19 times for providing the highest-quality medical care in Los Angeles. The Senior Administrative Assistant Performs a broad range of clerical, ad...
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...
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 ...
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 Coordinator III will serve as a member of the Clinical Research team. This position is responsible for coordinating and supporting the regulatory affairs activities encountered in clinical research trials conducted by the Clinical Research Center. Posting Summary Rutgers, The S...
Manage early-phase (1-2) oncology clinical trials. This preclinical-stage company leverages its proprietary platform to develop breakthrough therapies for solid tumors. Collaborate with CROs, vendors, and internal teams to ensure successful trial execution. Monitor trial progress and maintain regula...
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 successful Project Engineer/Manager candidate will be an energetic, proactive team collaborator who is accountable. The Project Engineer will have demonstrated experience in managing aspects of projects, working across agencies and organizations, and cultivating client relationships. Collaborate...
Manage a team of Project Managers/Senior Project Managers and support them with meeting their project delivery goals and perform people manager responsibility. Lead cross-functional project teams to deliver business critical projects by applying Waterfall, Agile and or Hybrid delivery methodology de...
ARE you able to identify and resolve potential scheduling conflicts and operational roadblocks? Are you great at keeping all stakeholders updated during a project, including leadership? Are you able to keep others on track and coordinate resources and people to complete the project? HERE at Core & M...
Solid understanding of data manipulation, data transformation, data cleansing, etc. Solid understanding of data manipulation, data transformation, data cleansing, etc. Data Visualization Analyst III. Talentry is looking for a professional who can take data and develop meaningful and impactful visual...
Department of Education, is hiring temporary, part-time research assistants to conduct classroom observations of preschool classrooms for a national research study. Research assistants will be paid to participate in the training and for time conducting observations and other research activities. SRI...
Assist the field Clinical Development team with administrative tasks for all clinical trials, including tracking study status and enrollment, managing research budgets, and maintaining up-to-date regulatory documents as required. Coordinate and organize clinical staff resources for internal research...
The Clinical Research Coordinator Supervisor (CRC-Su) functions independently and is responsible for the complete coordination of multiple assigned human subjects’ (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRC) responsibilities. Association of Cl...
The Clinical Research Coordinator II works independently providing study coordination including 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 e...