A Guide to Patient Recruitment and Retention is designed to help clinical research professionals improve the effectiveness of their patient recruitment efforts. Authored by Diana Anderson Ph.D., with contributions from 15 industry leaders, this 350-page manual offers real world, practical recruitment strategies and tactics grounded in facts and experiences. It is an invaluable resource for educating staff on patient recruitment, for managing recruitment initiatives for clinical trials, and for accelerating enrollment and retention efforts. Many sponsors and CROs now routinely distribute copies of this manual at investigator meetings.

Topics include:

• Trends and issues influencing patient recruitment, retention and ethics
• Benchmark data on patient volunteer demographics and recruitment costs
• Effective media strategies and tactics
• Budget considerations
• Guidelines on establishing new recruitment and retention practices
• Tips on effectively communicating with potential study subjects
• HIPAA Privacy Rules' impact on patient recruitment

Price: $79.00

Note: Special discount is available for bulk orders. Please send us an email to admin@helixresearchcenterworld.com or contact here, we will guide you to place the order accordingly.

The CRA's Guide to Monitoring Clinical Research is a valuable and practical educational resource for the individual readers and for group and staff training programs. Written by Karen E. Woodin, Ph.D., and John C. Schneider, this 400+ page book is an ideal resource for novice and experienced CRAs, as well as professionals interested in pursuing a career as study monitors.

The CRA's Guide explains the role and responsibilities of a CRA, informs readers of the history of the regulations, explains in detail the research process and describes the regulations and GCPs that govern clinical research.

Book topics:

• Preparing for a study and selecting investigators
• Obtaining and monitoring informed consent
• Preparing for a monitoring visit
• Recruiting and retaining study subjects
• Conducting adverse event and safety monitoring
• Preparing for audits and detecting fraud

Price: $79.00

Note: Special discount is available for bulk orders. Please send us an email to admin@helixresearchcenterworld.com or contact here, we will guide you to place the order accordingly.

Protecting Study Volunteers in Research

In addition to addressing current and emerging issues that are critical to our system of human subject protection oversight, Protecting Study Volunteers in Research has been expanded to include a chapter on how to implement the HIPPAA Privacy Rule in research. Protecting Study Volunteers in Research was designed to help organizations provide the highest standards of safe and ethical treatment of study volunteers. This manual will be routinely referenced for ethical considerations and insights, and for a comprehensive review of regulations and guidelines not conveniently found elsewhere.

Protecting Study Volunteers in Research has become required reading in many academic institutions, IRBs and investigative sites and is a suggested training resource by regulatory agencies and research sponsors. Biopharmaceutical and CRO companies have also made this manual mandatory reading for their staff

Price: $79.00

Note: Special discount is available for bulk orders. Please send us an email to admin@helixresearchcenterworld.com or contact here, we will guide you to place the order accordingly.

Becoming a Successful Clinical Research Investigator was created as a training resource for physicians and health professionals looking to break into the field of clinical research. It also provides helpful tips and techniques to clinical investigators interested in starting their own site or to anyone involved in the running of a clinical research site.

Written by Dr. David Ginsberg, with contributions from several other leading industry professionals, Becoming a Successful Clinical Research Investigator takes you through the process of determining whether clinical research is right for you to understanding the industry, setting up your own clinical research site and finding studies.

Book features:

• An explanation of the clinical research process
• The major players in the clinical research industry
• What to look for in hiring staff
• Establishing a budget for a clinical research site
• Regulatory requirements governing clinical research

Price: $79.00

Note: Special discount is available for bulk orders. Please send us an email to admin@helixresearchcenterworld.com or contact here, we will guide you to place the order accordingly.

The CRC's Guide to Coordinating Clinical Research was designed as a training resource for investigative site staff. Written by Karen E. Woodin, Ph.D., this 400-page guidebook is filled with valuable information on the role and responsibilities of a clinical research coordinator (CRC) and explains in detail the research process from the site and CRC perspective. The learning objectives for this activity are:

• Determine the role of the Clinical Research Coordinator at a clinical study site by describing the general responsibilities associated with that role.
• Identify the regulations governing clinical research.
• Describe the drug development process.
• Discuss Good Clinical Practices and how to apply them in clinical trials.
• Organize a clinical practice to manage clinical trials successfully to their completion

Price: $79.00

Note: Special discount is available for bulk orders. Please send us an email to admin@helixresearchcenterworld.com or contact here, we will guide you to place the order accordingly.