The Clinical Research Coordinator (CRC) will independently, or with general direction, execute, manage, and coordinate clinical research protocols, as directed by the Clinical Research Manager, Principal Investigator (PI), and/or the Associate Director of Clinical Research Programs for the Early Pha...
The Clinical Research Coordinator works directly with the Principal Investigator (PI), Co-Investigators (Co-I's), postdoctoral fellows, and trainees in the performance of duties related to the support and coordination of human subjects research. Certified Clinical Research Professional certification...
The Assistant Clinical Research Coordinator (Assistant CRC) works directly with the Principal Investigator (PI) and performs duties related to the support and coordination of research. Assistant Clinical Research Coordinator - Neuroscape Center. The Neuroscape Center at UCSF is looking for an Assis...
Assist Principal Investigators in the conduct of research by providing nursing expertise in the education and monitoring of patients involved in clinical trials and other research studies, in the collection and analysis of patient data, and in the preparation of research documents for the sponsoring...
I-SPY 2 TRIAL, which will involve the following: prepare protocol applications and informed consent forms for IRB submission, help design flow sheets, data forms and source documents; gather and interpret medical, surgical and laboratory data regarding clinical trial/study subjects; apply understand...
Under supervision, duties will include but not limited to: interpreting research protocols; recruiting subjects; screening for eligibility including scheduling subjects' visits; coordinating clinical, laboratory and data collection activities; processing and submitting laboratory specimens; collecti...
A company is looking for a Clinical Research Specialist - I (Assistant) to support clinical trials through operational planning and recruitment efforts. ...
This combined unit includes: 7 outpatient clinics, 4 inpatient services, a pulmonary function diagnostic center, 15 independent wet labs, 4 independent research service cores, 6 independent clinical research units, one specialty destination program, and the Nina Ireland Program in Lung Health focusi...
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....
Under the supervision of a Clinical Research Supervisor or Principal Investigator (PI), the incumbent will perform entry-level duties related to the support and coordination of clinical studies, and may receive training and development to prepare and advance for journey-level work at the next level ...
As part of Garber’s clinical research group, the postdoctoral researcher will work with numerous other faculty collaborators and eventually help to oversee and provide mentorship for the Clinical Research Coordinators and graduate students who ensure the day-to-day working operations of the trials, ...
Years of Experience: Typically requires 5 years of experience in clinical research, including a minimum of 2 years field monitoring experience and 3 years in lead CRA role. Excellent knowledge of medical terminology, protocol, clinical trial process, regulatory requirements, & company SOPs. ...
Provide initial clinical designs for future trials, partnering with research, translational oncology, biostatistics, clinical operations, regulatory, and pharmacology for input/alignment and presentation at the Therapeutic Development Team meetings. Medical Directors of Oncology Clinical Research – ...
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 Cedars-Sinai Biomedical Imaging Research Institute (BIRI) is an interdisciplinary research program established in 2010 to develop and apply state-of-the-art imaging technologies to today’s most pressing translational research and clinical questions. The Clinical Research Data Specialist I will w...
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. ...
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 ...
Masters Degree in clinical social work or marriage and family and child counseling, marital and family therapy, psychology, clinical or counseling psychology, or counseling with an emphasis in either marriage, family and child counseling or marriage and family therapy from an accredited school. Base...
The Clinical Research Associate II works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse, or Principal Investigator to coordinate and/or implement the study and may serve as the point of contact for the external sponsors. Works with a Clinical Researc...
The Associate Clinical Research III will assist in the clinical execution and management of all aspects of assigned clinical studies. Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial man...
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 ...
Under the supervision of Principal Investigator (PI), the clinical research coordinator (CRC) will perform duties related to the support and coordination of clinical research studies and may receive training and development to prepare and advance for journey-level work at the next level within the s...
The Fishbon Distinguished Professor will lead the development of a clinical research program at UCSF and SFCJL that will improve the care and health of older persons through the translation of research findings to clinical benefits in people with conditions associated with aging. Harris Fishbon Dist...
Experienced Clinical Research Coordinator (Dermatology/Skin Research). Perform other duties as assigned by the supervising Clinical Research Coordinator or management. Must have previous site-level research experience. Provide administrative assistance to the research team. ...
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...