The Clinical Research Nurse promotes good clinical practices in the conduct of clinical investigations by possessing knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protection. The Clinical Research Nurse is responsible for protocol coordi...
Whether you are healthy, or have a specific illness, we'll connect you with the right trial.Potentially get paid to access the most cutting edge medicines combating your disease.Most trials don't require much effort and will be located near you....
The Clinical Research Nurse is responsible for coordinating research protocols, including participant recruitment, enrollment, and follow-up. This position ensures compliance with federal regulations and guidelines for clinical trials and human subject protection. Effective communication with variou...
The CRN is a member of the clinical research team and assists in the recruitment, compliance and follow-up of patients that are eligible for, or registered to a clinical trial. Responsible for managing patient standard of care needs as well as participant and protocol needs through application of in...
Whether you are healthy, or have a specific illness, we'll connect you with the right trial.Potentially get paid to access the most cutting edge medicines combating your disease.Most trials don't require much effort and will be located near you....
Clinical Research Nurse The Clinical Research Nurse is responsible for coordinating research protocols, including participant recruitment, enrollment, and follow-up. Qualifications: Bachelor's Degree in nursing Current phlebotomy skills preferred Prior research experience preferred Registered Nurse ...
The Site Director performs clinical research activities as a Clinical Research Coordinator while also serving as Manager of clinical research staff at the Site. Recruits, trains, and mentors site staff, including Clinical Research Coordinators, Research Assistants, Administrative Assistants, Registe...
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 seeking a Clinical Research Coordinator I for the pediatric neurology clinical research center at Columbia University Medical Center. Additional responsibilities include maintaining compliance with existing policies and procedures at Columbia University, the IRB, FDA, NIH, and NYPH that relat...
The Clinical Research Nurse promotes good clinical practices in the conduct of clinical investigations by possessing knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protection. The Clinical Research Nurse is responsible for protocol coordi...
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. ...
Clinical research certification preferred. Provide study coordinator/datamanagement/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support andguidance in the clinical trials arena. ...
The Clinical Research Nurse promotes good clinical practices in the conduct of clinical investigations by possessing knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protection. The Clinical Research Nurse is responsible for protocol coordi...
The Clinical Research Nurse promotes good clinical practices in the conduct of clinical investigations by possessing knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protection. Scope of WorkThe Clinical Research Nurse is responsible for pr...
The Director of Clinical Research Operations is responsible for overseeing and managing all aspects of clinical research activities at the medical center. Leadership and Strategy: Develop and implement the overall clinical research strategy for the department under the direction of the Vice Dean of ...
Clinical Research Professional or Association of Clinical Research Professionals (ACRP) required for a minimum of 12 months prior to assuming CRC IV role. Provide experienced Clinical Research Coordinator (CRC) support to the Clinical Trials Office (CTO) and Multidisciplinary Team (MDT) team. Bachel...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
The Senior Research Coordinator (SRC) for the Transplant Clinical Research Center (TCRC) will report directly to the Director of Clinical Trials. The main role of the SRC will be to operate & maintain the day-to-day operational duties of their assigned clinical trials and clinical research study dat...
Under the supervision of the investigator(s) and research coordinator, and following established policies and procedures, performs a variety of clinical research activities, and participates in carrying out research objectives, ensuring compliance with all legal, regulatory and protocol guidelines. ...
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructio...
Provide study coordinator/datamanagement/regulatory specialist support to the Clinical Trials Office (CTO). Assist multidisciplinary team in research activities. ...
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...
Field monitoring of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to m...
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...
Required Bachelor's Degree in a health-related field, two or more years of clinical research experience, and National Research Certification within six months of hire OR five or more years of clinical research experience, and National Research Certification, OR clinical specialist with technician re...