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Clinical Trials Administrator   
Written for managers of clinical trials, each month Clinical Trials Administrator offers practical advice on the day-to-day issues
that impact you most.
Clinical Trials Administrator provides authoritative and practical guidance for the
full range of issues you face in managing clinical trials, including staff training, recruitment and retention; informed consent documentation; budgeting; developing and implementing protocols; and much more.
Each issue is meticulously written with objective and unbiased coverage bringing you case studies, expert analysis and practical advice, updates and management tools in a concise easy-to-use format.
A one-year subscription price including at least 12 issues per year is $299 plus $17.95 shipping and handling.
Here are some of the topics Clinical Trials Administrator will cover:
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Ongoing quality control
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Recruiting principal investigators
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IND safety reports
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Drafting privacy and authorization forms
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Informed consent: more than a signature
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Recruiting, training and retaining skilled CRCs
With your paid subscription, you will receive the opportunity to earn 15 nursing contact hours or 18 AMA PRA Category 1 Credits™.
Faculty: Stephen L. Kopecky, MD, Medical Director, Mayo Alliance for Clinical Trials, Rochester, MN; Elizabeth E. Hill, BSN, RN, DNSc, Assistant Professor, Director, Clinical Research, Management Program, Duke University School of Nursing, Durham, NC; Edwin V. Gaffney, PhD, Executive Director, Clinical Research, Baptist Health System Inc., Birmingham, AL; LaDale George, JD, Senior Counsel, Health Law Department/Health Care Business, Counseling Practicing Group, Foley & Lardner, Chicago; Ellen Hyman-Browne, JD, MPH, CIP, Office for Responsible Conduct of Research, Columbia University, New York City; Barbara LoDico, CIP, Executive Director, Human Subjects Protections, University of Medicine & Dentistry of New Jersey, Newark; Tamara Dowd Owens, RN, MSN, MBA, Clinical Research Manager, Governor's Institute on Alcohol and Substance Abuse, Research Triangle Park, NC; Lynette M. Schenkel, Director, Office for Responsible, Conduct of Research, University of Oregon, Eugene.
Objectives: The objectives of Clinical Trials Administrator are to:
- review pertinent regulatory mandates;
- develop practical clinical trial oversight strategies;
- review best practices shared by facilities that successfully conduct clinical trials.
Accreditation:
AHC Media LLC is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.
AHC Media LLC is accredited as a provider of continuing nursing education by the American Nurses Credentialing Center's Commission on Accreditation.
Credit Designation:
AHC Media LLC designates this educational activity for a maximum of 18 AMA PRA Category 1 CreditsTM. Physicians should only claim credit commensurate with the extent of their participation in the activity.
This activity is approved for 15 nursing contact hours using a 60-minute contact hour.
Provider approved by the California Board of Registered Nursing, Provider # 14749, for 15 Contact Hours.
Simply read the issues, answer the self-assessment questions at the end of each issue, compare your answers to the answer key, and review the source material relevant to any missed questions. Complete the evaluation form, which you'll receive at the end of each CME/CE semester, and mail it in. You'll receive your credit letter in the mail.
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You can review this product for 30 days. Your annual subscription includes published issues at no additional charge for the 12-month subscription period. 12 issues are expected. If you cancel your subscription within 30 days of receipt, you will receive a full credit upon receipt of request for cancellation.
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