On successful completion of this program, you will be certified and will have acquired knowledge, skills and competencies to start at an entry level role as Oncology Monitor (CRA) or similar.
Gain a comprehensive understanding of cancer biology, including the causes, risk factors, and global impact of the disease.
Develop skills in designing and implementing oncology clinical trials, including tumor grading, staging, and patient recruitment.
Develop skills in designing and implementing oncology clinical trials, including tumor grading, staging, and patient recruitment.
This first module introduces you to the foundational concepts of cancer and its treatment goals. You will learn about the definition, causes, and risk factors of cancer, as well as its global impact. This module also covers various treatment goals including cure, control, and palliation, providing a comprehensive understanding of cancer management.
Download the syllabus for a detailed overview of all lessons, assignments, reading materials, and a general overview.
✓ Understand the characteristics of cell formation, the major causes of cancer, and the global impact of the disease.
✓ Examine the impact of oncology studies and current treatment methods.
✓ Discuss available treatments and the objectives of treating cancer.
Patricia Hollis
in the industry for 21 years
This module offers a comprehensive understanding of various cancer treatments and their goals. Dive into the intricacies of chemotherapy, radiation, surgery, and advanced therapies, and explore complementary and alternative medicine. With expert guidance from Patricia Hollis, you’ll gain valuable insights into managing cancer treatments and their adverse reactions, equipping you with the knowledge to make informed decisions in clinical practice.
Download the syllabus for a detailed overview of all lessons, assignments, reading materials, and a general overview.
✓ Examine various cancer treatments and their adverse reactions.
✓ Explore alternative treatment options.
✓ Understand the principles behind different therapeutic approaches.
✓ Gain insights into patient management during cancer treatments.
Patricia Hollis
in the industry for 21 years
This module will deepen your knowledge in the field of cancer treatment. You’ll delve into the intricate details of chemotherapy and radiation, exploring their mechanisms, uses, and impacts. Gain a comprehensive understanding of the most common cancer drugs, the principles behind their use, and the delicate balance of risks versus benefits in tumor therapies.
Download the syllabus for a detailed overview of all lessons, assignments, reading materials, and a general overview.
✓ Identify common cancer drugs and cancer combinations.
✓ Thoroughly understand the relationship between risk and benefits of tumor therapies.
✓ Recognize chemotherapy drug types and different principles.
Patricia Hollis
in the industry for 21 years
This advanced module is designed to enhance your understanding of tumor grading and staging systems, crucial tools in oncology. You will delve into the intricacies of how tumors are classified and staged, providing a foundation for treatment decisions and prognosis evaluation. With guidance from an expert instructor, Patricia Hollis, you will master these essential concepts to improve your clinical research capabilities.
Download the syllabus for a detailed overview of all lessons, assignments, reading materials, and a general overview.
✓ Understand the concepts of Tumor Grades.
✓ Learn the different systems used for tumor grading and staging.
✓ Explore the significance of tumor classification in treatment planning and prognosis.
✓ Gain insights into the methodologies and criteria for assessing tumor progression.
Patricia Hollis
in the industry for 21 years
Unlock the complexities of oncology trials with this expert-level module. Dive deep into the intricate designs of oncology studies, exploring the nuances that make these trials unique. With guidance from Patricia Hollis, an esteemed expert in the field, you will gain comprehensive knowledge and practical skills essential for designing and managing successful oncology studies.
Download the syllabus for a detailed overview of all lessons, assignments, reading materials, and a general overview.
✓ Discuss Oncology trial schematics and understand the design features.
✓ Describe the four phases of Oncology studies.
✓ Understand endpoint requirements in Oncology.
Patricia Hollis
in the industry for 21 years
This module is designed to provide you with comprehensive knowledge of clinical assessments, especially within the context of oncology trials. You will gain a deep understanding of various assessment methods, from tissue sampling to advanced imaging techniques, and how these tools are used to evaluate and monitor patient progress.
Download the syllabus for a detailed overview of all lessons, assignments, reading materials, and a general overview.
✓ Recognize common clinical assessments related to oncology trials.
✓ Gain proficiency in reviewing clinical reports and interpreting assessment results.
✓ Identify disease history and understand common Inclusion/Exclusion criteria.
Patricia Hollis
in the industry for 21 years
In this advanced module, you’ll dive deep into the intricate world of oncology, focusing on the different lines of therapies used in cancer treatment. You’ll gain a comprehensive understanding of the various therapy approaches, including single and combination treatments, as well as adjuvant and neo-adjuvant therapies. This module is designed to provide you with the knowledge and skills necessary to navigate the complexities of cancer dosing and dose escalation.
Download the syllabus for a detailed overview of all lessons, assignments, reading materials, and a general overview.
✓ Define each line of therapy and understand the timing of each line.
✓ Understand dosing design in oncology studies.
✓ Explore single and combination therapies and their applications.
✓ Differentiate between adjuvant and neo-adjuvant therapies.
✓ Comprehend palliative therapy and its role in patient care.
Patricia Hollis
in the industry for 21 years
This advanced module is designed for experienced clinical researchers aiming to deepen their understanding of adverse events, dose-limiting toxicity, and dose modifications. Through this module, you will gain expertise in identifying, reporting, and managing adverse events to ensure patient safety and data integrity in clinical trials, particularly in oncology studies.
Download the syllabus for a detailed overview of all lessons, assignments, reading materials, and a general overview.
✓ Recognize the most common adverse events and discuss clinical events related to oncology studies.
✓ Understand the risk assessment and reporting requirements for adverse events and SAEs.
✓ Learn the methodologies for dose-limiting toxicity and dose modifications.
✓ Develop the ability to conduct thorough risk assessments.
✓ Gain insights into the common toxicities and the DLT process.
Patricia Hollis
in the industry for 21 years
Navigating the complexities of oncology subject identification and the enrollment process is critical for the success of clinical trials. This module delves into the intricacies of recruiting oncology subjects, from initial screening procedures to confirming eligibility and cancer diagnosis. Led by expert instructor Patricia Hollis, you will gain valuable insights and practical knowledge to enhance your clinical research skills in this specialized field.
Download the syllabus for a detailed overview of all lessons, assignments, reading materials, and a general overview.
✓ Discuss recruitment challenges in Oncology studies.
✓ Describe the screening and enrollment process.
✓ Understand the role of the medical monitor and various key members during the screening.
Patricia Hollis
in the industry for 21 years
This module is designed to enhance your expertise in managing and analyzing critical clinical documents. You’ll delve into the essential elements of pathology and radiology, gaining a comprehensive understanding of clinical reports and source documents. This knowledge is crucial for accurate data interpretation and decision-making in oncology studies.
Download the syllabus for a detailed overview of all lessons, assignments, reading materials, and a general overview.
✓ Become familiar with Pathology, Radiology, and Clinical reports and source documents.
✓ Understand MRIs and CTs and their role in oncology studies.
✓ Identify critical data in source documents related to cancer results.
Patricia Hollis
in the industry for 21 years
This advanced module will provide you with comprehensive knowledge on the Response Evaluation Criteria in Solid Tumors (RECIST). You’ll delve into the intricacies of tumor measurement and response evaluation, critical for oncology clinical trials. Through detailed lessons and practical assignments, you’ll learn to accurately assess disease progression, enhancing your proficiency in clinical research.
Download the syllabus for a detailed overview of all lessons, assignments, reading materials, and a general overview.
✓ Distinguish between RECIST 1.0 and RECIST 1.1.
✓ Utilize appropriate oncology disease progression algorithms.
✓ Understand disease progression thoroughly.
Patricia Hollis
in the industry for 21 years
Delve into the specialized world of oncology research with this comprehensive module. You’ll gain a deep understanding of the unique infrastructure of oncology sites and how it impacts the Delegation of Responsibility log. Prepare to tackle the challenges of monitoring at these sites by learning about the key roles and functions of site staff. This module, guided by expert instructor Patricia Hollis, will equip you with the knowledge and skills to effectively manage oncology research sites.
Download the syllabus for a detailed overview of all lessons, assignments, reading materials, and a general overview.
✓ Prepare for challenges with site structure and Delegation of Responsibility at oncology sites.
✓ Describe key site staff and associated roles.
✓ Discuss the key function of site staff.
Patricia Hollis
in the industry for 21 years
This comprehensive module is designed to equip you with the expertise required to excel as an Oncology Monitor. Delve into the intricate details of sponsor and CRO requirements, understand the profound psychological impacts of the role, and discover practical tips and tricks to navigate the unique challenges of monitoring oncology studies. This course offers an in-depth exploration that ensures you are prepared to meet the demands and excel in your role.
Download the syllabus for a detailed overview of all lessons, assignments, reading materials, and a general overview.
✓ Learn Sponsor/CRO expectations of Oncology Monitors
✓ Understand the stress and pressures of monitoring oncology studies
✓ Learn time-saving techniques while monitoring
Patricia Hollis
in the industry for 21 years
This exam will help you apply your newly acquired knowledge and skills, covering a wide range of topics from the certificate program to ensure your readiness for a position in clinical research.
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There are several reasons why you might consider becoming a clinical research associate who specializes in oncology trials:
According to the US Bureau of Labor Statistics, the median annual salary for clinical research coordinators and monitors (which includes CRAs) was $71,490 as of May 2020. However, salaries can range from around $44,600 to over $126,000 per year. Glassdoor, a website that provides salary information based on user-submitted data, reports an average base salary of $76,697 per year for clinical research associates with a focus on oncology trials in the United States. However, this figure may not be representative of all regions, employers, or levels of experience.
Continual learning opportunities: As a CRA working in oncology trials, you will have the opportunity to learn about the latest advancements in cancer treatment and research. This can be an exciting and intellectually stimulating career path that allows you to continually develop your knowledge and skills.
Overall, becoming a CRA who specializes in oncology trials can be a rewarding and fulfilling career path that provides you with the opportunity to make a meaningful impact in the fight against cancer, while also offering competitive salary, continual learning opportunities, and career advancement potential.
The typical responsibilities of a CRA focusing on oncology trials can vary depending on the stage of the trial and the specific employer, but generally include the following:
Overall, the responsibilities of a CRA focusing on oncology trials are multifaceted and require strong organizational, communication, and problem-solving skills, as well as an in-depth understanding of clinical research principles and regulations.
Upon enrollment you will receive your first certification “Confirmation of Enrollment”. After successful completion of the course and your exam, you get your personal “Course Certificate” including:
We also show you how to best share your certificate on LinkedIn and other social media platforms.
There are several reasons why you might consider getting a CRA certification:
Demonstrated knowledge and commitment: Obtaining a CRA certification demonstrates to employers and colleagues that you have a strong understanding of clinical research processes, regulations, and best practices. It shows your commitment to your career in clinical research and can set you apart from other candidates when applying for jobs.
Increased job opportunities: Many employers prefer or require candidates with CRA certifications for their open positions. Having a certification can make you a more competitive candidate and increase your job opportunities.
Career advancement: A CRA certification can help you advance in your career by opening up opportunities for promotion, leadership roles, and increased pay.
Continuing education: Many employers require ongoing education and professional development, which can help you stay up-to-date with the latest developments in the field.
Overall, obtaining a CRA certification can help you stand out in a competitive job market, demonstrate your knowledge and commitment to your career, and open up opportunities for career advancement and professional development.
No, you can proceed with the course in your own pace. But please keep in mind, that you might have to purchase a course extension in order to continue learning (check the pricing table above).
To become a CRA, you will typically need a bachelor’s degree in a life science or healthcare-related field, such as biology, chemistry, nursing, or pharmacy. However, some employers may accept degrees in other fields if you have relevant work experience.
In addition to a degree, it is beneficial to have experience working in the healthcare or research industry. This can include positions such as a research assistant, laboratory technician, or nurse. Other skills for a CRA include attention to detail, strong organizational and communication skills, the ability to work independently and as part of a team, and problem-solving abilities. Proficiency in Microsoft Office and other relevant software is also important.
If you are not sure if this is the right training for you, we are happy to help you make the right decision. Email us at academy@viares.com and we will contact you.
The Oncology CRA
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Verified ownerGreat 👍 and relevant information
Verified owner
Verified ownerIt has been apleasure
Verified ownerJust finished the VIARES CRA Academy and I’m blown away. Clear, practical, straight-to-the-point lessons that actually prepare you for the real job. Passed the exam first try. Best investment I’ve made in my career. Highly recommend!
Thank you VIARES
Verified ownerReally good work and presentations. I wish live also be a part of it. Otherwise the course is excellent
Verified ownerVIARES ACADEMY ALL-In-One Accelerator
Verified ownerClinical Research Associate Accelerator
Verified ownerClinical Research Associate
Verified ownerClinical Study Coordinator II
