Advanced Package

5 Clinical Research Training Courses – SAVE 61%

Experience the full power of the VIARES Clinical Research training courses. Get upskilled on advanced professional competencies to speed up your clinical research career.

Why speed up my Clinical Research career?

A Growing Industry

First, the clinical research industry is growing every year by 6-8%. In parallel, the global talent pool grows by about 4-5%, which provides great career opportunities. 

If you have the required degree and work experience, it’s your turn to become one of these knowledgeable experts!

 

Jobs That Pay Well

The number of job opportunities is currently growing. As an example salaries for CRA start at around €35.000 in Europe and $75.000 in the USA and go way above $100.000 per year.

Next to these starting salaries,  it is possible to take fast career pathways and gain more responsibilities rapidly. Promotions often come within 2-3 years into professional levels, taking salaries up to about €45.000 in Europe and $100.000+ in the USA.

Description

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 boost your clinical research career.

The training includes access to all academy services, and an industry recognized professional certification.

You can start the training right away and complete it within the given timelines at your own pace. This training contains over 500 hours of online material and you can complete it at your own pace.

You do not need to wait for a kick-off date, you can start your training anytime  – as early as today if you wish.

Requirements:

This program will be of benefit to anyone with a life science degree and relevant work experience, ideally in clinical research, pharma or related areas, e.g. working with patients, medical products or services, medical technology, laboratories or similar.

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.

Certificates:

  • VIARES, GCP

Life-time payment plan includes:

  • all benefits from the monthly payment plan with only one payment
  • PLUS – unlimited life-time access to your training course
  • PLUS – free download of your training course handouts for offline learning
 

Monthly payment plan includes:

  • registration fee
  • all online-training course material
  • online access to our learning management system
  • mini-exams during the training to test your knowledge
  • VIARES exam – 2 attempts included
  • personalized certificate upon completion
  • join career events at no cost
  • free access to our weekly updated global job list
  • apply to exclusive job offers
  • get your personal career coaching
  • any time free cancellation of monthly payment

WE TRAIN AND CERTIFY YOU

The VIARES Clinical Research ADVANCED Package consists of 5 training courses. Successfully complete the courses to obtain five certificates.

CLINICAL RESEARCH ASSOCIATE

  • Background of medicines development
  • Research and discovery stage & product development
  • Clinical development
  • Regulatory submission, Health Technology Assessment, lifecycle management
  • ICH GCP and other applicable regulations
  • Applicable international and national regulations
  • ICH GCP E6 (R2)
  • FDA Regulation
  • Quality Assurance: Audits and Inspections
  • The Study Protocol
    • Elements of a Study Protocol according to ICH GCP
    • Trial Design
    • Methodologies
  • Roles and Responsibilities
    • Ethics Committees
    • Sponsor / Monitor
    • Investigator
    • Competent Authority
  • Selecting an Investigational Site
    • Assessing Investigational Sites
    • Training and Upgrading Investigational Sites
  • Initiating Investigational Sites
    • Organizing the Initiation Visit
    • Setting up the required documentation – Essential Documents
  • Effective Monitoring
    • Planning, Conducting, Documenting, and Reporting Monitoring Visits
    • Managing Issues
  • Closing Investigational Sites
    • Organizing the Close-Out Visit
    • Documentation
    • Reporting
  • Patient Protection
    • Patient Information
    • Collecting Patient Consent
    • Special Patient Populations
  • Adverse Event Reporting
    • Types of Adverse Events
    • Identifying and Reporting Serious Adverse Events
  • Managing the Investigational Medicinal Product
    • Definition of investigational medicinal product (IMP) / study drug
    • Provision of the IMP
    • Drug Accountability
    • Randomization, blinding and un-blinding processes
    • Managing Expiry Dates
    • Collecting IMP after Site Close-out
  • Data Collection
    • Clinical Research Form (CRFs)
    • Process of Data Collection
    • Data Collection Systems
  • Data Validation
    • Data validation process
    • Query Process
    • Data Quality Assurance

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.

After successful completion of the exam, you will be graduating the VIARES program and obtain your certificate.

REMOTE & CENTRALIZED MONITORING

  • Background of monitoring concepts
    • Including on-site, remote, and statistical monitoring
  • Regulatory guidance to remote and statistical monitoring
  • Monitoring concepts in the framework of risk-based monitoring
  • From concept to reality: Remote monitoring and centralized statistical monitoring
  • Daily Life of a Remote Monitor
    • Responsibilities
    • Tools and resources
    • How to handle centralized statistical monitoring
    • Monitoring activity and their focus
    • Documentation and follow-up
    • Team interactions
  • What makes a good Remote Monitor

The VIARES Certification is an online exam covering 40+ questions from the VIARES training course. You need to complete the exam within 60 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.

After successful completion of the exam, you will be graduating the VIARES program and obtain your certificate.

THE ONCOLOGY CRA

  • Understand the characteristics of cell formation, the major causes of cancer and global impact of the disease
  • Examine the impact of Oncology studies and current treatment
  • Be able to discuss available treatments and objectives of treating cancer
  • Examine various cancer treatments and their adverse reactions
  • Explore alternative treatment options
  • Identify common cancer drug and cancer combinations
  • Thoroughly understand the relationship between risk and benefits of tumor therapies
  • Recognize chemotherapy drug types and different principles
  • Differentiate between cancer and uncontrolled tumor growths
  • Recognize the six major categories of cancer classifications
  • Understand components of medical terminology related to cancer
  • Be able to discuss Oncology trial schematics and understand the design features.
  • Be able to describe the four phases of Oncology studies.
  • Understand Endpoint requirements in Oncology
  • Recognize common clinical assessments related to oncology trials
  • Gain proficiency in reviewing clinical reports
  • Identify disease history and common Inclusion/Exclusion criterion
  • Define each line of therapy and understand the timing of each line
  • Understand dosing design in oncology studies
  • Recognize most common Adverse Events and be able to discuss clinical events related to oncology studies
  • Recognize common toxicities and understand the DLT process
  • Be able to discuss recruitment challenges in Oncology studies
  • Describe the screening and enrollment process
  • Understand the role of the medical monitor and various key members during screening process
  • Pathology
  • Radiology
  • Clinical Reports and Source
  • Medical
  • Surgical
  • Distinguish between RECIST 1.0 and RECIST 1.1
  • Utilize appropriate oncology disease progression algorithms
  • Understand disease progression
  • 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
  • Learn Sponsor/CRO expectations of Oncology Monitors
  • Understand the stress and pressures of monitoring oncology studies
  • Learn time saving techniques while monitoring

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.

CLINICAL DATA MANAGEMENT

  • Identify concepts in ethical reasoning which may influence our analysis & results from data.
  • Understand the process of data curation, & the custodial duty of data science. Learn some essential tools used by data scientists.
  • Investigate & manipulate data to learn its metadata, shape & robustness.
  • Identify an appropriate chart & present data to illustrate its core characteristics.
  • Recognise the importance & process for applying concepts of privacy & anonymity.
  • Integrate methods for metadata & archival into data management.
  • Investigate data distribution & confidence, & reshape using Pandas.
  • Illustrate core analysis with histograms & box plots.
  • Determine implications in collection, mining & recombination of open- & digital data.
  • Employ methods for presenting data for synthesis & usage, & employing methods for data maintenance.
  • Perform techniques in randomness & probability to understand distribution & likelihood.
  • Apply histograms, line charts & scatter plots to illustrate probability.
  • Acknowledge the privacy & confidentiality issues in data storage & security of personal data.
  • Recognise responsibilities & mechanisms for securing data-at-rest & data-in-motion.
  • Apply linear & continuous sampling methods to assess normal distributions.
  • Plot distributions as normal histograms & continuous curves.

The VIARES Certification is an online exam that covers questions from the related 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.

CLINICAL RESEARCH PROJECT MANAGER

  • Get familiar with project management terminology.
  • Define project success criteria.
  • Set up project phases correctly.
  • Choose fitting tools to manage a project.
  • Communicate efficiently while managing a project.
  • Understand typical differences between the PM’s role depending on the company type.
  • Understand the stakeholder landscape.
  • Analyse stakeholders.
  • Identify key stakeholders.
  • Communicate successfully with different stakeholders choosing adequate style, frequency, and the level of detail.
  • Understand the project external and internal environment.
  • Assess how the environmental factors affect the project.
  • Define requirements to make the project a success story.
  • Define the project scope.
  • Build a strong project definition.
  • Obtain the approval for your project definition.
  • Differentiate risks, constraints, and issues.
  • Identify project risks and decide on a suitable primary response strategy.
  • Analyse project risks in three dimensions – likelihood, impact, and detectability.
  • Quantify risks and calculate the Risk Priority Number.
  • Optimise conditions for high risks.
  • Monitor risks and keep them under control.
  • Assess the effectiveness of your risk management process.
  • Understand the regulatory framework for risk management in clinical studies.
  • Apply general risk management principles and procedures on clinical projects.
  • Develop the Clinical Risk Management Plan.
  • Use adequate tools to manage clinical study risks efficiently.
  • Communicate effectively with functional teams to manage clinical study risks successfully.
  • Identify key stages of a project.
  • Analyse whether something is missing for a successful delivery (gaps).
  • Plan how to bridge the gaps.
  • Assign responsibilities to your team members.
  • Develop the clinical study budget.
  • Prepare a detailed realistic plan (baseline schedule) of the project including milestones, critical path, work breakdown, and allocated resources.
  • Use a well-designed baseline schedule to measure progress and manage the project in the execution phase.
  • Monitor study progress.
  • Identify early signs of the project falling behind or going astray compared to the plan.
  • Apply measures to keep the project on track.
  • Apply measures to maintain GCP and regulatory compliance.
  • Control study costs and handle out-of-scope requests.
  • Manage and support your team during audits and inspections.
  • Manage CAPA plans effectively and efficiently.
  • Contribute to the timely development of the CSR.
  • Avoid project drift by proper planning, strong management, and clear communication.
  • Set project completion criteria and produce an adequate Project Acceptance Checklist.
  • Lead the close-out meeting.
  • Evaluate the project – what went well, what went wrong and why, derive lessons learnt.

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.

After successful completion of the exam, you will be graduating the VIARES program and obtain your certificate.

Hear from our graduates

Dasa

Dasa

I work as a Pediatrician at a University Hospital, where we run several clinical trials. I wanted to broaden my horizon in the field of Clinical Research. The VIARES Academy CRA Course offered me valuable perspectives in this area.

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It is definitely an advantage for my future career.

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Zdravko

Zdravko

I’m glad to share that I was part of VIARES Clinical Research Talent Program. VIARES CRTP is well balanced which gives you new skills and opportunity to be part of the huge CRA’s family. The program contains well-organized micro – courses,

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webinars which are prepared by true professionals. Thank you for that scientific journey.

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reviews curated by judge.me

-61%

BESTSELLER

Advanced Package
This Course includes

 349,90

 34,90 / month for 12 monthsPay monthly

ERIC KLAVER

Trained in 6 continents

Eric brings with him 20 years of experience training and meeting management and has worked in clinical research for almost 25 years. The global reach of this experience (Eric has trained in six continents) makes him the partner of choice to work with. Eric combines soft skills with personal responsibility in every training.

GAVIN CHAIT

Data Scientist at Whythawk

Gavin Chait is a Data Scientist at Whythawk, which specializes in integrated open data consulting, and training for open knowledge, freedom of information, and economic development projects. He spent more than a decade in economic and development initiatives in South Africa. He was a commercial director at the Open Knowledge Foundation, and led the implementation of numerous open data projects around the world. Gavin has twenty years of experience in teaching at all academic levels, and is a passionate advocate for knowledge development through open access to data and freedom of information.

KAMILA NOVAK

certified Lead Auditor for ISO 9001:2015

Kamila Novak, MSc, has been involved in clinical research since 1995, having worked in various positions in pharma and CROs. Since 2010, she has been working as an independent consultant in medical writing, auditing, training, project and risk management. She delivered dozens of courses in areas related to clinical research and project management. In August 2019, Kamila became a certified Lead Auditor for ISO 9001:2015. Kamila is a Core Team Member in the DIA GCP & QA, Clinical Research, and Project Management Communities.

PATRICIA HOLLIS

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.

BARTEK JAROSZ

18 Years experience

Bartek has 18 years experience in clinical research business, mostly spent at largest global Contract Research Organizations. At Quintiles he was responsible for pioneer development of clinical start-up and regional contract departments. He served as executive member of clinical start-up leadership team at INC Research, acting as global head of site contract division. His most recent experience includes support for pharmaceutical organizations in various project specific roles. Bartek enables biopharma to get their sites up and running faster. He is author of several training programs about site contract related matters and successfully delivered to hundreds of individuals worldwide.

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  • VIARES exam – 2 attempts included
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  • Online access to our learning management system
  • No training course handouts for offline learning
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  • No training course handouts for offline learning
  • No unlimited access

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