Responsible for researching study participating recruitment, screening, and enrollment,
coordinating clinical research studies, organizing files and records, and other assigned duties.
Not exact matches
The
research comes from the Infant Brain Imaging
Study (IBIS), a collaborative effort by investigators at the Montreal Neurological Institute, and four clinical sites in the United States, coordinated to conduct a longitudinal brain imaging and behavioural study of infants at high risk for au
Study (IBIS), a collaborative effort by investigators at the Montreal Neurological Institute, and four
clinical sites in the United States,
coordinated to conduct a longitudinal brain imaging and behavioural
study of infants at high risk for au
study of infants at high risk for autism.
The
study is
coordinated by the Brain
Research Unit at the
Clinical Research Centre of the University of Eastern Finland.
Through regional networks in the U.S. like the Pediatric Neuromuscular
Clinical Research (PNCR) Network and Project Cure, and international organizations such as the International Coordinating Committee (ICC) and TREAT - NMD, the SMA community has collaborated effectively on recruiting patients, establishing standards of care, standardizing outcome measures, and supporting multi-site clinical efforts, such as the Biomarkers for SMA (BforSMA) and the PNCR Network Natural History
Clinical Research (PNCR) Network and Project Cure, and international organizations such as the International
Coordinating Committee (ICC) and TREAT - NMD, the SMA community has collaborated effectively on recruiting patients, establishing standards of care, standardizing outcome measures, and supporting multi-site
clinical efforts, such as the Biomarkers for SMA (BforSMA) and the PNCR Network Natural History
clinical efforts, such as the Biomarkers for SMA (BforSMA) and the PNCR Network Natural History
studies.
NEW YORK and SAN FRANCISCO, March 28, 2017 — The Parker Institute for Cancer Immunotherapy, Bristol - Myers Squibb Company (NYSE: BMY) and the Cancer
Research Institute (CRI) today announced a multi-year clinical research collaboration to coordinate and rapidly initiate clinical Immuno - Oncology (I - O) studies across the Parker Institute and CRI n
Research Institute (CRI) today announced a multi-year
clinical research collaboration to coordinate and rapidly initiate clinical Immuno - Oncology (I - O) studies across the Parker Institute and CRI n
research collaboration to
coordinate and rapidly initiate
clinical Immuno - Oncology (I - O)
studies across the Parker Institute and CRI networks.
In the second
study, researchers from the Keenan
Research Center for Biomedical Science at St. Michael's Hospital in Toronto, Canada, looked at inconsistencies between
clinical and autopsy diagnoses in more than 1,000 people listed in the National Alzheimer's
Coordinating Center database.
Subsequently, she
coordinated various
research studies with the Veterinary
Clinical Investigation Center at the University of Pennsylvania.
Successfully
coordinating and managing up to 11
clinical research studies at a time throughout their full life cycle from subject recruitment to
study completion.
Highly motivated and efficient with superior knowledge of the methods, processes, and techniques used in
clinical research with ability to
coordinate research studies.
Position Overview A
Clinical Research Associate is responsible for planning, designing, coordinating and conducting all activities required to initiate, monitor, and complete clinical research
Clinical Research Associate is responsible for planning, designing, coordinating and conducting all activities required to initiate, monitor, and complete clinical research
Research Associate is responsible for planning, designing,
coordinating and conducting all activities required to initiate, monitor, and complete
clinical research
clinical research research studies.
A
Clinical Research Associate is responsible for planning, designing, coordinating and conducting all activities required to initiate, monitor, and complete clinical research
Clinical Research Associate is responsible for planning, designing, coordinating and conducting all activities required to initiate, monitor, and complete clinical research
Research Associate is responsible for planning, designing,
coordinating and conducting all activities required to initiate, monitor, and complete
clinical research
clinical research research studies.
I am an expert when it comes to participating in specialty clinics,
coordinating with
clinical staff and physicians to evaluate patients who are considered for
research studies.
Nurse Researcher Penn Medicine, Hampton, GA 10/2012 — Present • Provide and
coordinate clinical care for patients involved in
clinical research studies • Ascertain accuracy of data collection and data recording, and handle correlating follow - up • Schedule evaluation screenings and ensure that all participant are made physically and mentally ready for them • Provide patient participants with information on what to expect during
clinical trials • Handle administration of investigational drugs, and handle detailed
clinical assessments •
Study chronic and acute diseases and disorders, and assist in developing new treatment plans • Assist in testing new treatments and medications that may change the way diseases and disorders are perceived • Compile
clinical data and review and assess it for reporting purposes
Demonstrated ability to support the management and
coordinate the tasks of multiple
clinical research studies.
To work effectively with a team of
research professionals to manage
clinical trials and
coordinate the
study process at investigative sites from
study initiation through close - out.