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. Works closely with a regulatory coordinator or directl...
The Clinical Services Coordinator, Intermediate (CSC) will report directly to the supervisor of care management support operations and will serve as initial point of contact for providers and members in the medical management process by telephone or correspondence. ...
We are seeking an experienced Clinical Research Coordinator to join our team who will be responsible for overseeing clinical trials to test the effectiveness of new drugs and biotechnology. Clinical Start Up Meeting, Clinical Planning Meeting, Site Initiation Meeting. The CRC will be responsible for...
The Clinical Trial Supply Coordinator will be responsible for managing the supply chain activities for clinical trials, ensuring that all necessary materials and supplies are available for the successful execution of clinical studies. Clinical Trial Supply Coordinator for a fulltime, contract-to-per...
As a Clinical Research Coordinator I, you will work independently providing study coordination including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Our team of scientists develop s...
With minimal supervision, the Clinical Research Coordinator II (CRC-II) is responsible for providing coordinator support to multiple human subjects’ (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRC) responsibilities. Association of Clinical Research...
The Clinical Services Coordinator Intermediate will report to the CHP Manager. The Children’s Health Program (CHP) team provides identification, referrals, and care management for all Medi-Cal members under years old and collaborates within Promise Clinical Team. In this role you will work with cli...
The Specialty Resource Coordinator - RN is responsible for coordinating assigned surgical specialty services within the Main OR and in the Procedure Center; to function as an expert practitioner (circulator role) whose intuition and skill arise from comprehensive knowledge thoroughly grounded in exp...
We are seeking a highly motivated and organized Clinical Research Coordinator (CRC) to join our team in Pasadena, CA. As a CRC, you will work closely with clinical teams, patients, and sponsors to facilitate the successful execution of clinical research projects. Clinical Research Coordinator or sim...
With minimal supervision, the Clinical Research Coordinator II (CRC-II) is responsible for providing coordinator support to multiple human subjects’ (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRC) responsibilities. Association of Clinical Research...
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. Works closely with a regulatory coordinator or directl...
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 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 looking for a Data Entry Specialist whose main function is providing excellent customer service by quickly and accurately processing submissions sent electronically by our members.A Data Entry Specialist will compare data with source documents submitted by our members, checking for accuracy a...
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...
Plays a key role in optimized product delivery accountable for all the project management aspects of various projects from simple to complex in nature. Conducts project meetings and is responsible for the definition and implementation of project risk mitigating measures. Selects project methodology ...
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. ...
Under the direction of Research Institute Management, the Clinical Research Nurse Coordinator II is responsible for providing coordinator assistance for sponsored clinical studies within the Center for Clinical Research in accordance with Institutional policy, Good Clinical Practice and ICH guidelin...
Job Number: J0924-0131 Job Title: Clinical Team Manager - Peri-Operative Services, FT (J0924-0131) Job Type: Full-Time Permanent Location: General Site, 4001 Leslie Street Job Category: Management Date Posted: October 21, 2024 Closing Date: November 18, 2024 Salary: $121,169. Clinical Team Manager, ...
Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a minimum of 3 years’ experience in monitoring pharmaceutical industry clinical trials. Have an in-depth knowledge of Good Clinical Practice, ICH g...
We are looking for an enthusiastic, self-driven, and collaborative Research Associate II / Senior Research Associate. Join our dynamic Biologics research group focused on pioneering novel oncology therapeutics within a thriving biotech start-up. ...
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...
The Project Coordinator is responsible for administering and organizing all types of projects, from simple activities to more complex plans. The Project Coordinator is responsible for ensuring that assigned projects are completed on time, within budget and meet quality standards. In this role, he/sh...
The Registered Nurse/Quality Program Coordinator, Stroke/Sepsis will support the Director in maintaining and revising the Quality and Performance Improvement (QPI) program, projects, and initiatives across the Hospital. The coordinator also promotes the QPI program to medical, nursing, and support s...
As a Clinical Research Associate focused on medical devices, you will play a crucial role in the planning, execution, and monitoring of clinical trials. You will ensure that studies are conducted in accordance with regulatory requirements, Good Clinical Practice (GCP), and company policies. Assist i...