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.
To become an Oncology CRA, there are several educational and professional backgrounds that can be beneficial. Here are some examples:
Overall, a background in a relevant scientific field, coupled with experience in clinical research, knowledge of relevant regulations, and strong soft skills can be beneficial in preparing for a career as a CRA focusing on oncology trials.
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.
Obtaining a certificate as a CRA focusing on oncology trials can be beneficial for several reasons:
Overall, obtaining a certificate as a CRA focusing on oncology trials can be beneficial for career advancement, professional development, networking, and standardization. It can help demonstrate your expertise in clinical research and improve your job prospects in this growing field.
This is a snapshot of the latest new entries from our full list of global clinical research jobs. Our list is updated and curated for you daily, adding hundreds of new jobs. Get full access with a VIARES account.
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| Position – click to go to job | Company | Location | Date Created | Source | Title | Id (key) |
A Flexible Online Setup
Our setup enables you to complete this program either next to a full-time job or in a focused effort. 100% of the program is online and most of the training courses can be completed at any time.
Get Certified & Job Ready
On successful completion of this program, you will be certified and will have acquired knowledge, skills and competencies to start monitoring Oncology trials.
The VIARES Oncology Monitor training course is more than just a training. It’s a life-changer!
Enjoy all our services during your program enrollment.
Certificates:
Life-time payment plan includes:
Monthly payment plan includes:
The VIARES Certification is an online exam covering 100 questions from the VIARES training course. You need to complete the exam within 90 minutes and achieve at least 80% of all points to be graded positive. You have two attempts, of which the attempt with the higher score is applied for your certification.
This program is designed for talents who wish to advance their career as Oncology Clinical Research Associate.
Is this academy right for me? We are happy to help you make the right decision.
Email us at academy@viares.com and we will contact you.
VIARES Clinical Research Academy provided me with great exceptional opportunity to explore and gain knowledge & skills in clinical research, the training is conducting by highly professional trainers, the training materials attracted my interests
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and guided me to seek deeper extra related knowledge. My interest in clinical research became greater, I am eager to start my career in clinical research and to contribute efficiently in this interested sector.
At this occasion I would present my gratitude and thankfulness to VIARES Academy staff and team members, you are doing great job.
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It was a very interactive course! I liked it! The topics were very enriching and very organized. The moderators were very knowledgeable. I loved the assignments; they made me think harder! I was also privileged to get the one year membership
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with ACRP and I also completed the ELKA which was very enjoyable. Thanks to the VIARES team.
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Grow your career into a Project Management with you new skills on Project Management Basics, Stakeholder Management, Project Planning, Project Risk Management, Clinical Risk Management,...
The role of a clinical study coordinator is critical to the success of any medical research study or clinical trial. 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 Clinical Study Coordinator or similar.
Start your clinical research career as Clinical Trials Assistant. Get certified and acquired knowledge, skills and competencies to start at an exiting clinical research career as Clinical Trials Assistant or similar.
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in the industry for 21 years
Patricia has been in the clinical research industry for 21 years. She began her career as a clinical research coordinator at the Medical College of Virginia where she coordinated pharmaceutical and PI initiated trials. She has been a Clinical Research Associate for 16 years and has had the opportunity to serve as a Lead CRA, Clinical Trial Manager, Auditor, Mentor, and Clinical Research Instructor. She has worked in all phases of research and is experienced in numerous therapeutic areas, including Oncology, Endocrinology, CNS, Immunology, Cardiology, Nephrology and Device. Currently, she is a contract CRA through her company, The Hollis Group, LLC, which she owns with her husband and serves as a consultant at local research sites. Patricia completed a Bachelor of Science degree at Virginia Commonwealth University, MBA at Texas Woman’s University and has had specialized oncology training from the Oncology of Nursing Society.
