Facilitate clinical testing and check results to determine patient eligibility for a clinical trial. GENERAL SUMMARY:Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research ...
Responsible for facilitating research studies; providing knowledgeable information regarding each research protocol to the medical and nursing staff; evaluating the eligibility of potential candidates for research studies; assisting in the informed consent process; monitoring research study complian...
Clinical Research Coordinators. Clinical Research Coordinators are responsible to coordinate and manage multiple studies. IMPROVE THE FUTURE AS OUR CLINICAL RESEARCH COORDINATOR!!!. We have been nationally acknowledged for our diligence to provide the highest quality of data for our clinical researc...
Provide experienced Clinical Research Coordinator (CRC) support to the Clinical Trials Office (CTO) and Multidisciplinary Team (MDT) team. Clinical Research Professional or Association of Clinical Research Professionals (ACRP) required for a minimum of 12 months prior to assuming CRC IV role. Bachel...
The Clinical Research Coordinator will support multiple research studies (government, private and pharmaceutical) through the coordination and implementation of clinical trials and protocols involving human subjects. Facilitate screening, enrollment, and treatment of research subjects in compliance ...
We are seeking a full-time Clinical Research Coordinator with a minimum of 1 year of clinical experience, for our Additionally, someone with a strong interest in the Clinical Research field would be an excellent fit for our...
Facilitate clinical testing and check results to determine patient eligibility for a clinical trial. Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research protocol are met...
Provide study coordinator/datamanagement/regulatory specialist support to the Clinical Trials Office (CTO). Assist multidisciplinary team in research activities. ...
Clinical Research Coordinator - Department of Pharmacy Practice. Clinical Research Coordinator - Department of Pharmacy Practice. POSITION PURPOSE Coordinate and participate in clinical research studies by performing activities involved in the collection, compilation, documentation of research data....
Facilitate clinical testing and check results to determine patient eligibility for a clinical trial. Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research protocol are met...
Clinical Research Coordinator Responsibilities. Minimum 5+ years of directly related experience in clinical research and clinical trials is necessary. Will serve as the central administrative coordinator, facilitating communication across research teams, sponsors, and other stakeholders across the d...
Clinical Research Coordinator I The CRC I will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. Liaising with Laboratory team...
The Clinical Research Coordinator provides research coordination support for multiple clinical research projects. The Clinical Research Coordinator position will primarily support task-oriented needs. The position involves coordinating various clinical research projects, such as registries, retrospe...
Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. Bachelor's degree in Clinical Research, Biology, Chemistry, Nursing or other closely related field. Previous coordinator experience preferred. Department: Cancer Clinical & Trans...
Facilitate clinical testing and check results to determine patient eligibility for a clinical trial. Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research protocol are met...
Assist study team with aspects of clinical research coordination including: identifying potential subjects, screening subjects, consenting and enrolling subjects, and collecting and managing patient and laboratory data for clinical research subjects. There is a need to move, transport, and position ...
Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. Bachelor's degree in Clinical Research, Biology, Chemistry, Nursing or other closely related field. Previous coordinator experience preferred. Department: Cancer Clinical & Trans...
The Clinical Research Coordinator will support multiple research studies (government, private and pharmaceutical) through the coordination and implementation of clinical trials and protocols involving human subjects. Responsible for screening, enrollment, and treatment of research subjects in compli...
Responsible for facilitating research studies; providing knowledgeable information regarding each research protocol to the medical and nursing staff; evaluating the eligibility of potential candidates for research studies; assisting in the informed consent process; monitoring research study complian...
Knowledge equivalent to that which normally would be acquired through a four year college degree program in a clinical field such as health or biological science and a minimum of one to three years of related and progressively more responsible or expansive work experience in clinical and/or research...
Provide experienced Clinical Research Coordinator (CRC) support to the Clinical Trials Office (CTO) and Multidisciplinary Team (MDT) team. Clinical Research Professional or Association of Clinical Research Professionals (ACRP) required for a minimum of 12 months prior to assuming CRC IV role. Bachel...
Barrington James is looking for Clinical Research Coordinators in multiple locations within Michigan to join our client. This is a 3-6 month contract opportunity, this is a great opportunity to build a professional relationship with the client and to grow into other positions within the Clinical Res...
Facilitate clinical testing and check results to determine patient eligibility for a clinical trial. Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research protocol are met...