Prior to her work at Sabin, Stoever spent several years
managing clinical research studies in cancer and infectious diseases.
Not exact matches
The
study, «Acceptance and Commitment Therapy to
Manage Pain and Opioid Use after Major Surgery: Preliminary Outcomes from the Toronto General Hospital Transitional Pain Service,» is published in the Canadian Journal of Pain, by first author Muhammad Azam, Ph.D. candidate at York University and senior authors Dr. Joel Katz, Affiliate Scientist, Toronto General Hospital
Research Institute (TGHRI) and Dr. Hance Clarke, Director of the Transitional Pain Service at TGH, UHN and
Clinical Researcher, TGHRI.
«This
study demonstrates that CRFA is an effective long - term therapeutic option for
managing pain, and improving physical function and quality of life, for patients suffering from painful knee osteoarthritis when compared with intra-articular steroid injection,» according to the
clinical trial report by Leonardo Kapural, MD, PhD, of the Center for Clinical Research, Winston - Salem, N.C., and col
clinical trial report by Leonardo Kapural, MD, PhD, of the Center for
Clinical Research, Winston - Salem, N.C., and col
Clinical Research, Winston - Salem, N.C., and colleagues.
Congress has questioned how NIH is
managing its
Clinical and Translational Science Awards, which support
research such as this aging
study at the University of Kansas.
Miller, who serves as director of
clinical research and executive vice-chair of Emergency Medicine at Wake Forest Baptist, said the
study built on previous
research findings that more complex patients
managed in an observation unit with stress CMR testing experienced a reduction in care costs of about $ 2,100 per patient per year.
Duke
Clinical Research Institute (DCRI) has launched a patient registry to help researchers and clinicians identify,
manage and
study people who have a progressive lung disease called idiopathic pulmonary fibrosis.
The BRSC
manages the resource commitment associated with
clinical studies, including supporting compliance with regulatory directives governing
research in Human Subjects.
Successfully coordinating and
managing up to 11
clinical research studies at a time throughout their full life cycle from subject recruitment to
study completion.
Medical Affairs executives, particularly Vice Presidents, combine commercial - side business meetings with a charter to supervise
research strategy,
manage clinical studies, and validate scientific claims supporting specific products.
2014 - present • Oversee entire recruitment process: finding and screening potentially suitable subjects for relevant
studies, and ensuring proper protocol for obtaining and documenting consent is followed through • Communicate and collaborate with laboratories and investigators on findings, and report on
clinical research results • Conduct and monitor
studies to ensure proper procedures are carried through in compliance with company policies and federal and state regulations • Counsel health care professionals on proper treatment and dosages •
Manage all researchers and acquire necessary space and equipment to conduct
studies
Use Microsoft Access and Excel to enter data collected on
study participants from the Computer - Assisted Personal Interview (CAPI) and abstract
clinical information from their Electronic Medical Records (EMR) which is entered in Discovere, a web - based
research platform used to
manage and analyze
study data.
Some of the duties of a
clinical research assistant include
managing the front desk, organizing
research files, assisting with
research studies and programs and verifying
research data.
Expertise in QC of documents, remote Monitoring and supporting the management by handling the tasks of multiple
clinical research studies managing eTMF's & designing Clinical Portfolio's from Spon
clinical research studies managing eTMF's & designing
Clinical Portfolio's from Spon
Clinical Portfolio's from Sponsor end.
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.
QUALIFICATIONS SUMMARY
Study Manager and
Clinical Development Scientist with 10 years extensive pharmaceutical industry experience managing Phase II - IV clinical research
Clinical Development Scientist with 10 years extensive pharmaceutical industry experience
managing Phase II - IV
clinical research
clinical research studies.