Clinical Research Coordinator II. A minimum of 1 year experience in clinical research required, preferably in coordination of clinical research projects. Clinical Research Project Planning and Preparation. Develop patient rapport to explain research protocols and minimize protocol violations. ...
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...
Research Director of the Clinical Research Unit (CRU) and. Coordinate all research activities related to the Research Network at assigned. The Clinical Research Nurse Coordinator is responsible for. Investigators/Research Meetings. ...
The Clinical Research Coordinator oversees the day-to-day functions of multiple clinical research studies. Providence Clinical Research Coordinator - Santa Monica, California. Two years: Experience in a Clinical Research setting. ...
The Senior Clinical Research Coordinator plays a critical role in the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The ideal candidate is an experienced professional or leader who has direct responsibility for the implemen...
Mathematical skills sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets. Bachelor’s degree or 1-3 years of previous study coordination or clinical research coor...
The Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. Two years: Experience in a Clinical Research setting. ...
The Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The Clinical Research Coordinator collaborates with the Principal Investigator (PI), ancillary departments, central 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. Responsible for compiling and reporting on e...
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...
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 Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The Clinical Research Coordinator collaborates with the Principal Investigator (PI), ancillary departments, central research...
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. Work alongside physician-scienti...
The Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The Clinical Research Coordinator collaborates with the Principal Investigator (PI), ancillary departments, central research...
Under the direction of the Manager of Development Operations, this position supports the Development Department in which principal responsibilities include researching, analyzing and providing high-level research on high-net-wealth individuals, corporations and foundations using a variety of biograp...
Overseeing the smooth execution of internal research studies, including scheduling, recruitment, patient consent, and administering questionnaires. Manage IRB submissions and study progress for internal and external research studies and ensure that documentation and requirements are up to date. Appr...
The Senior Clinical Research Coordinator plays a critical role in the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The ideal candidate is an experienced professional or leader who has direct responsibility for the implemen...
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...
Responsible for all aspects of clinical research from initiation through completion of research projects with human subjects. One year of research experience. Demonstrated track record of human subjects research coordination, informed consent procedures and documents. Has knowledge in human subjects...
Clinical Research Associate II. Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements. We translate unique clinical, medical affairs and commercial i...
Qualifications: - Bachelor’s degree in Human Services field or equivalent.Experience in conducting standardized assessments - Experience in working with patients with substance use disorders - Primary care experience preferred....
Bachelors degree with 4+ year experience as a Clinical Trials Associate; or Associate's degree with 7+ years' experience as a Clinical Trials Associate; or 10+ years clinical research experience. Participate in clinical research teams to ensure the most effective and efficient conduct of clinical re...
Clinical Program Coordinator RN - Cath Lab (full time day shift). Collects and compiles clinical data for cardiac patients concurrent with patient stay in hospital. Category:Healthcare, Keywords:Healthcare Program Coordinator, Location:Santa Monica, CA-90411. ...
The Associate, Analytical Sciences will manage routine testing, including cell culture, multi-parametric flow cytometry, immunoassay, and cell-based functional assays, to characterize engineered T cell therapy processes and products. ...
This series covers interdisciplinary 0801/1301 Research General Engineer/Research Physical Scientist positions which are managing, supervising, leading, and/or performing professional research engineering work or work in the research physical sciences and may include work in a combination of physica...