The Coordinator for the Weight Loss/Orthopedic Surgery Program acts as a clinical liaison and resource for the in-hospital aspects of the programs. For over 50 years, Doctors Hospital of Manteca has provided superb clinical care to patients in the Central Valley of California. We strive to deliver t...
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...
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...
The Coordinator for the Weight Loss/Orthopedic Surgery Program acts as a clinical liaison and resource for the in-hospital aspects of the programs. For over 50 years, Doctors Hospital of Manteca has provided superb clinical care to patients in the Central Valley of California. We strive to deliver t...
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...
Provide clinical supervision and training. ...
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...
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...
Under supervision of the Educational Clinical Coordinator, timely and effectively meets agency and program timelines for clinical documentation, compliance trainings, assigned project deadlines, submission of timecards, and respond to phone calls, emails, texts, and chats. The Associate Educational ...
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 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. Works closely with a regulatory coordinator ...
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...
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...
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. ...
This is a high travelling, on-site monitoring contract Clinical Research Associate opportunity for a West-Coast based Contractor. ...
If you are an experienced regional CRA looking to join a global leader in clinical research with a reputable sponsor aligned program, this is a good time to apply with ICON PLC. Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for ...
Research Associate – Scientist I, Biology. The successful candidate will be a hands-on cell and molecular biologist, bringing valuable research expertise and skills to our organization. Reporting to the Associate Director of Translational Medicine, the candidate will play a key role in supporting on...
Join Refiberd as a Research Associate and play a crucial role in transforming the fashion industry toward a circular economy. ...
LEGARZA PROGRAM SPECIALIST - FULL TIME AND PART TIME POSITIONS AVAILABLE. We are in search of a motivated go-getter who has the skills and determination to develop, grow, and manage a phenomenal sports program. As we continue to expand, we need a quality person who believes in our values and has the...
We are seeking an enthusiastic and motivated Research Associate who will support the nonclinical and process development of one or more novel drug products. Prior experience in chemical synthesis and analytical techniques in a research or production setting. Able to conduct research with careful att...
As a Senior Research Associate, you will be responsible for developing and optimizing HPLC methods, conducting qualitative and quantitative analyses, and supporting various research and development projects. Perform routine and advanced HPLC analysis to support research and development activities. T...
As a Clinical Research Associate you will be responsible for a variety of monitoring tasks and you will have a chance to work on clinical studies in different therapeutic indications, ensuring the clinical trial is conducted in compliance with study protocol and procedures, ICH-GCP guidelines and th...
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. ...
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...
They will also effectively monitor and present project updates to relevant stakeholders, clients, or project team members. The ideal candidate will be responsible for planning, coordinating, and implementing projects within the decided-upon budget, timeline, and scope. Update relevant stakeholders o...