The Trusted Standard in Research, Ethics, and Compliance Training The Collaborative Institutional Training Initiative (CITI Program) is dedicated to serving the training needs of colleges and universities, healthcare institutions, technology and research organizations, and governmental agencies, as they foster integrity and professional advancement of their learners. CCRPS is uniquely positioned to provide accredited certification courses for entry level professionals due to our in-depth level of content provided. Certified Clinical Research Professionals Society Corp. (CCRPS) is a not-for-profit 501 (c)(3) professional society providing accredited certification and training for entry-level and mid-level clinical research professionals. This course focuses on the theoretical underpinnings of clinical research and the practical aspects of conducting clinical trials: the rationale for design features of Phase I, II, and III trials, recruitment of participants, techniques for randomization, data collection and endpoints, interim monitoring, and results reporting. By the end of the course, students should have the knowledge and skills required to design and undertake a clinical trial. All rights reserved © 2020 Certified Clinical Research Professionals Society Corp. clinical research associate training and placement, Boston, MA, Clinical Research Associate Certification, Clinical Research Coordinator Certification. Recruiters are paid by the company which hires you and thus are free for searching employees. Bedside Nursing: Want to Write a Research Protocol? ", Bedside Nursing "From Clinical Inquiry to Conducting Nursing Research", OHRP’s Thinking on Key Revisions to the Common Rule, Creating and Sustaining Diverse Study Enrollment: Towards a Quantifiable Science of Recruitment, Applying the Principles of the Science of Safety to Improve Subject Safety in Clinical Research: Actionable Practices to Identify and Minimize Risk, The Evolution of Vulnerability – The Ethics of Equitable Subject Selection, Including Vulnerable Subjects with Cognitive Impairment in Research, Minimally Disruptive Research: A Respectful Approach to Conducting Clinical Studies, The Evaluation of Evidence for Regulatory Decision Making, Recent Advances in the Early Detection of Alzheimer's Disease, Affordable Care Act and Research: Where Have We Been and Where Are We Going, An Update from the Patient-Centered Outcomes Research Institute (PCORI), Utilizing the Research Ehtics Review Process as a Method to Incorporate Quality by Design. Be realistic but also be driven. This course provides the foundational knowledge upon which one can develop his/her competence as a clinical research professional. Explore 359,967 research studies … The 12 modules included in the course are based on ICH GCP Principles and the Code of Federal Regulations (CFR) for clinical research trials in the U.S. The Good Clinical Practice (GCP) course is designed to prepare research staff in the conduct of clinical trials with human participants. Stata). Students can apply for partial scholarships or enroll for a payment plan for CRA and CRC certification courses. Study materials provided for non-Clinical Trials modules may include study guides, textbooks, CD-ROMs/additional computer software (e.g. Browse the latest online clinical trials courses from Harvard University, including "HMX Pro Immunology: Immuno-oncology" and "Principles and Practice of Clinical Research." This highly practical course explores the relevance of clinical research in drug development and summarises the ethical and regulatory requirements for clinical trials. Read reviews to decide if a class is right for you. Plenty of situational examples will be provided in order to maximize understanding and clarity. This course teaches the basic skills of project management derived from PMI principles but with focus on clinical trials. In this course we will cover and discuss the – often very complex – legal rules and principles for contracts in clinical trials as well as the requirements as a result of these contracts. The Site has extensive information on funding and training opportunities, clinical trials, health news and links to the many … It has become increasingly more important to use solid project management principles when managing clinical trials. We provide clinical research associate, clinical research coordinator, clinical research assistant, ICH GCH, pharmacovigilance drug safety, and international clinical research certifications accredited and peer reviewed by the ACCRE. SOCRA's online courses are intended to provide access to training and continuing education that will promote quality clinical research, protect the welfare of research participants and improve global health. Many of the courses are conducted online, or are hybrid programs with both online classes and in-person workshops. What You Should Know Before the FDA Arrives, Risk Based Monitoring from the Site Perspective, cGMP for Investigational New Drugs (IND) in Phase 1 Clinical Trials, Regulatory Updates for Clinical Research Professionals. Healthcare professionals can also receive ACPE, AMA/ACCME, ANCC, and ICPE continuing education credits through our clinical research online training. Welcome. The Graduate Certificate in Clinical Trials Research aims to build research capacity through a formal qualification and improve the quality of the conduct of trials. Below are links we readily refer to graduates who are looking for job support. Compliance with GCP assures patients and the public that the rights, safety and wellbeing of people taking part in studies are protected and that research data is reliable. Healthcare professionals can also receive ACPE, AMA/ACCME, ANCC, and ICPE continuing education credits through our clinical research online training. Certificate in Pharmaceuticals and Clinical Trials Management (Online) (This certificate is a fully Hybrid-Online version of the traditional Certificate in Pharmaceuticals and Clinical Trials Management certificate. Efficiently identify and report safety events in your clinical trials. The purpose of this course is to introduce you to the process and procedures of monitoring a clinical trial as a clinical research associate working for a pharmaceutical or device manufacturer (known as the sponsor). Our mission is to support clinical trials by providing accessible education to entry and mid level professionals. You can move freely between the two formats as long as all four courses are completed in sequential order. You can demo all of our courses for free by clicking … Design and Interpretation of Clinical Trials: Johns Hopkins UniversityDrug Development Product Management: University of California San DiegoData Management for Clinical Research: Vanderbilt UniversityUnderstanding Clinical Research: Behind the Statistics: University of Cape TownAI in Healthcare: Stanford University GCP protects the rights, safety and wellbeing of study participants. 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