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The Complete CenterWatch Training Series

The Investigator's Guide to Clinical Research
A Guide to Patient Recruitment and Retention
Protecting Study Volunteers in Research
The CRC’s Guide to Coordinating Clinical Research
The CRA's Guide to Monitoring Clinical Research
eClinical Trials: Planning and Implementation
How to Grow Your Investigative Site


	The Investigator's Guide to Clinical Research New Third Edition with New Content Book content covers... Reviewing the clinical development process Understanding the regulatory requirements Identifying and securing clinical grants Conducting and managing a clinical trial Preparing for FDA audits
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	A Guide to Patient Recruitment and Retention Book content covers... Understanding patient recruitment ethics Implementing new media strategies and tactics Analyzing benchmark data on patient volunteer demographics and recruitment costs Reviewing therapeutic-specific case studies
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	Protecting Study Volunteers in Research New Third Edition with New Content Book content covers... The historical perspectives on human subject research Understanding the regulatory requirements and ethical principles Understanding the diverse role and responsibilities of institutions and the investigator in human subject research and the study process
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	The CRC’s Guide to Coordinating Clinical Research Book content covers... CRC responsibilities, problems and opportunities Regulations and good clinical practices (GCPs) Writing and implementing standard operating procedures (SOPs) Preparing for a study, including case report forms (CRFs), site evaluations, investigator meetings, monitoring visits and more Adverse events and safety monitoring Sample forms, logs and checklists
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	The CRA's Guide to Monitoring Clinical Research Book content covers... Selecting qualified investigators Preparing for a study Obtaining and monitoring Informed Consent Conducting adverse event and safety monitoring Preparing for audits and detecting fraud Preview selected book sections!
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	eClinical Trials: Planning and Implementation Book content covers... Understanding how eCT technology can accelerate and improve clinical research processes Redesigning research processes to optimize the advantages of various eCT technologies Establishing quantatative metrics to track the impact of eCT technology implementation Understanding and applying the intent of 21CFR11 and data privacy requirements Comprehending the value of data interchange standards Please note this publication is being discontinued: 40% off remaining stock
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	How to Grow Your Investigative Site Book content covers... Expanding operations and infrastructure Identifying and retaining clinical research staff Negotiating budgets and contracts Managing site financials and recruitment costs Expanding your pipeline with more research grants Please note this publication is being discontinued: 40% off remaining stock
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