Sentences with phrase «trials research committee»

«I was honored to be nominated as a candidate for treasurer and thrilled that I won,» said Cohn, who is also chair of the clinical trials research committee at the University of Chicago.

Not exact matches

Contributors: Members of the writing committee for this paper were Peter Brocklehurst (professor of perinatal epidemiology, National Perinatal Epidemiology Unit (NPEU), University of Oxford; professor of women's health, Institute for Women's Health, University College London (UCL)-RRB-; Pollyanna Hardy (senior trials statistician, NPEU); Jennifer Hollowell (epidemiologist, NPEU); Louise Linsell (senior medical statistician, NPEU); Alison Macfarlane (professor of perinatal health, City University London); Christine McCourt (professor of maternal and child health, City University London); Neil Marlow (professor of neonatal medicine, UCL); Alison Miller (programme director and midwifery lead, Confidential Enquiry into Maternal and Child Health (CEMACH)-RRB-; Mary Newburn (head of research and information, National Childbirth Trust (NCT)-RRB-; Stavros Petrou (health economist, NPEU; professor of health economics, University of Warwick); David Puddicombe (researcher, NPEU); Maggie Redshaw (senior research fellow, social scientist, NPEU); Rachel Rowe (researcher, NPEU); Jane Sandall (professor of social science and women's health, King's College London); Louise Silverton (deputy general secretary, Royal College of Midwives (RCM)-RRB-; and Mary Stewart (research midwife, NPEU; senior lecturer, King's College London, Florence Nightingale School of Nursing and Midwifery).

All study participants gave written informed consent and the study was approved by the Monash University Human Research Ethics Committee (approval number CF12 / 0348 -2012000146), and the trial registered with the Australia and New Zealand Clinical Trial Registry (registration number 12611000468trial registered with the Australia and New Zealand Clinical Trial Registry (registration number 12611000468Trial Registry (registration number 12611000468921).

Consent for the current GM trials being undertaken by Leeds University, the Sainsbury Laboratory and Rothamsted Research was granted in accordance with the Environmental Protection Act 1990 following evaluation by the Advisory Committee on Releases to the Environment (ACRE).

But Tsiri Agbenyega, head of the Malaria Research Unit at Komfo Anokye Hospital in Kumasi, Ghana and chairman of the RTS, S Clinical Trials Partnership Committee, remains optimistic.

In a report published earlier this month, the French committee says: «Contrary to all recognised rules for medical research, the first trials on humans were done even though experiments on animals were still extremely limited.»

In addition to Boschi, those facing trial are: Franco Barberi, committee vice president; Bernardo De Bernardinis, at the time vice president of Italy's Civil Protection Department and now president of the country's Institute for Environmental Protection and Research; Giulio Selvaggi, director of the National Earthquake Centre; Gian Michele Calvi, director of the European Centre for Training and Research in Earthquake Engineering; Claudio Eva, an earth scientist at the University of Genoa; and Mauro Dolce, director of the office of seismic risk at the Civil Protection Department.

In the same week that the trial was approved, the Medical Research Council announced that it was to set up its own committee to oversee its work in gene therapy.

Despite this uncertainty, the Department of Health decided last week to allow the UK Coordinating Committee on Cancer Research to seek local approval for the trial at each centre taking part.

The report from an international committee convened by the U.S. National Academy of Sciences (NAS) and the National Academy of Medicine in Washington, D.C., concludes that such a clinical trial «might be permitted, but only following much more research» on risks and benefits, and «only for compelling reasons and under strict oversight.»

In this role, Ms. Roxland re-launched and chaired J&J's Ethics Committee, created an enterprise - wide consultation service for teams and individuals confronting complex research ethics issues, and provided guidance on issues such as post-trial access for former research participants, conducting clinical trials in war - torn regions, testing of a potential Ebola vaccine during a public health crisis, commercialization of stem cell therapies, subject recruitment and withdrawal, and expanded access / compassionate use.

He was the founding Chairman of the Multiple Myeloma Research Consortium, Clinical Trials Core and now chairs the Multiple Myeloma Committee for the Alliance for Clinical Trials in Oncology (the former CALGB).

In addition, they integrate their research objectives with those of the Biomarker Sciences Program committees to incorporate predictive / prognostic molecular and imaging biomarkers into therapeutic trials, whenever possible.

Berman faculty have led or served on committees of the National Academy of medicine related to human and to animal research and led work for the National Cancer Institute creating model national guidance on informed consent; Berman faculty have served on multiple Data Safety and Monitoring Boards for federally and privately funded trials including the recent NIH sponsored ebola trials.

Professional Associations Monroe County Bar Association, Member New York State Bar Association, Chairman: Torts, Insurance, and Compensation Law Section (2003 - 2004) NYSBA Automobile Liability Committee Chairman (1991 - 1995) NYSBA House of Delegates, Delegate (1999 - 2004) New York State Trial Lawyers Association Risk and Insurance Management Society (2007 - present) Council on Litigation Management (2008 - present); Chairman, Products Liability Conference (2010 - 2013) New York Editorial Board, Lawyers Cooperative Publishing Company (1993 - 1995) Defense Research Institute (2000 - present) The National Fire Protection Association, Member The American Society for Metals, Member

He is a member of the American Bar Association and its Torts / Insurance Committee, the New York State Bar Association, Defense Research Institute, Primerus Defense Institute and co-chairs its Insurance Coverage & Bad Faith Group, the Nassau County Bar Association and its Grievance Committee, the Nassau - Suffolk Trial Lawyers Association, New York Claims Association and Nassau Suffolk Claim Managers Council.

Levinson also serves as chair of the section's Practice Resources Committee, which compiles documents such as pleadings, research, expert reports and other information that might be helpful to fellow trial lawyers.

Affiliations: Bar Association of the District of Columbia District of Columbia Bar, Litigation Section, chair of the Steering Committee, 1993 — 1995 Virginia Bar Association Fairfax Bar Association American Board of Trial Advocates The Barristers (Washington, DC) DC Defense Lawyers» Association, president, 2001 — 2002 Women's Bar Association Defense Research Institute American Bar Association National Retail Federation National Council of Chain Restaurants

Serving as a Research Associate for Endometrin Pharmaceuticals, conducting research into new drugs designed to treat type 2 diabetes; creating trial protocols, working closely with ethics committees, verifying data, and writing detailed reports of fResearch Associate for Endometrin Pharmaceuticals, conducting research into new drugs designed to treat type 2 diabetes; creating trial protocols, working closely with ethics committees, verifying data, and writing detailed reports of fresearch into new drugs designed to treat type 2 diabetes; creating trial protocols, working closely with ethics committees, verifying data, and writing detailed reports of findings.

Clinical Research Associates can work on various stages of a clinical trial, performing tasks such as creating trial protocols, developing trial methodology, collaborating with ethics committees, liaising with doctors running the trial, making visits to the trial site, ordering supplies, monitoring expenses, and authenticating data collection forms.

Usual work activities described in a Clinical Research Associate resume example include creating trial protocols, collaborating with ethics committees, recruiting assistants, verifying data, writing visit reports, presenting results, and writing final reports.

Key Accomplishments • Created and implemented a clinical investigation plan which increased efficiency by 50 % • Trained 15 research assistants in handling site initiation, closeout and interim monitoring work • Introduced 8 different clinical trial committees, including clinical events committee, data safety monitoring board and steering committee • Obtained 3 informed consents for human research subjects which were in limbo for 5 years

PROFESSIONAL EXPERIENCE University of South Florida, Tampa • FL 2008 — Present Clinical Research Administrator / Project Manager Manage and coordinate all aspects of clinical trials and network committees at the Data Coordinating Center (TNCC) within the Pediatrics Epidemiology Center (PEC) under a federally awarded grant TrialNet for Type 1 Diabetes.

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This pragmatic trial was designed in accordance with the consolidated standards of reporting trials guidelines54 and was conducted by a research team independent of the programme, with an independent trial steering committee including chairman, parental representation and members with expertise in statistics; early years» intervention studies; and child psychiatry.