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VIARES Academy
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Clinical Study Coordinator II

On successful completion of this program, you will be certified and will have acquired knowledge, skills and competencies to advance your career as Clinical Study Coordinator.

Increase salary potential by €52 EUR-80k+.
100% Money-back Guarantee with 5 Day Refund Policy.

COURSE Content

Successfully complete the 8 competency modules below to obtain your VIARES Academy Certificate.
  • ALCOA-CCEA Principles
  • Source DocumentsTypes
  • Correction Methods
  • Schedule of Events
  • Informed Consent Form (ICF)
  • Informed Consent Process
  • Elements of an ICF
  • Medical History
  • Source Documentation
  • Concomitant Medication (ConMeds
  • Schedule of Events
  • Source Documents
  • Inclusion/Exclusion Criteria
  • Eligibility
  • ConMeds
  • Medical History
  • Source Documentation
  • ConMeds
  • Medical History
  • Adverse Events (AE) and Serious Adverse Events
  • Day 3 procedures
  • New AE/ConMeds
  • Medical History/AE/ConMeds reconciliation
  • Protocol Deviations
  • Day 7 procedures
  • New AE/ConMeds
  • Medical History/AE/ConMeds reconciliation
  • Protocol Deviations
  • Day 14 procedures
  • New AE/ConMeds
  • Medical History/AE/ConMeds reconciliation
  • Protocol Deviations
  • Day 28 procedures
  • New AE/ConMeds
  • Medical History/AE/ConMeds reconciliation
  • Protocol Deviations

VIARES CERTIFICATE

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:

  • course title
  • contact hours
  • continuing education units (CEU)
  • your overall course score
  • date of completion
  • personal certificate verification code
 

We also show you how to best share your certificate on LinkedIn and other social media platforms.

Getting a certification as an advanced clinical study coordinator can provide several benefits, both for your career and for the clinical research industry as a whole. Here are some reasons why you might want to consider getting certified:

  • Professional credibility: Earning a certification demonstrates your commitment to professionalism and competence in the field of clinical research. Certification can also demonstrate to employers and colleagues that you have a high level of knowledge and expertise in your field.
  • Career advancement: Certification can increase your marketability and give you a competitive edge in the job market, as well as potentially increasing your earning potential. Many employers may prefer or require certification for advanced clinical study coordinator roles.
  • Industry recognition: Certification can also contribute to the standardization and recognition of the clinical research profession, helping to establish consistent standards and best practices in the field.
  • Continuing education: The certification program can help you stay up-to-date on the latest developments in the field and expand your knowledge and skills.
  • Personal and professional growth: Pursuing certification can be a challenging and rewarding experience, helping you to develop new skills and expand your knowledge, as well as contributing to your personal and professional growth.

Delivered by industry experts

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PATRICIA HOLLIS

Clinical Operations Expert

Hear from our graduates

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Aparna

The VIARES Talent Program opened the doors to the fascinating world of clinical trials and covered all aspects of the field. The course was very well-organized and detailed. The instructors were knowledgeable, enthusiastic, and provided real-world

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insights. The assignments really helped to internalize all we had learned throughout the course.

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Darina

I am very grateful for the opportunity to participate in the VIARES Clinical Research Talent program. The program is well developed and structured. Courses, knowledge checks, assignments and webinars are very useful for understanding

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the whole clinical trial process. I have learned a lot of new things. I will definitely use it in my career. I recommend it to anyone who is interested in the field of clinical trials.

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WHY BECOME an advanced clinical study coordinator?

There are several reasons why you might consider becoming an advanced clinical study coordinator:

  • Impact on patient health: As an advanced clinical study coordinator, you would play a critical role in helping to bring new treatments and therapies to patients. By coordinating clinical trials, you would be contributing to the development of potentially life-saving treatments and helping to improve the quality of life for patients.
  • Career growth and advancement: As an advanced clinical study coordinator, you would have the opportunity to take on more complex and challenging studies, work with a wider range of stakeholders, and develop new skills and expertise. This could lead to career advancement opportunities, such as becoming a project manager or clinical research associate.
  • Job security: The demand for skilled clinical study coordinators is high, and this is likely to continue as the pharmaceutical industry grows. This means that there is likely to be job security and opportunities for career advancement in this field.
  • Competitive salary: Advanced clinical study coordinators are typically well-compensated, with salaries that are competitive with other healthcare professions. The salary of an advanced clinical study coordinator can vary depending on a number of factors, such as the location, level of experience, industry, and employer. According to data from the Bureau of Labor Statistics (BLS), the median annual wage for clinical research coordinators, which includes advanced clinical study coordinators, was $53,000 as of May 2020 in the United States. However, salaries can range from around $40,000 to over $80,000 per year, with many coordinators earning in the range of $50,000 to $70,000. Experienced coordinators, those with advanced degrees, or those working in the pharmaceutical industry may earn higher salaries. Overall, the salary of an advanced clinical study coordinator can be competitive, with potential for growth and higher compensation over time as you gain more experience and responsibility.
  • Flexibility: Many clinical study coordinators work in a variety of settings, including hospitals, research institutions, and pharmaceutical companies. This means that there may be opportunities to work in a setting that is convenient and fits your lifestyle.

 

Overall, becoming an advanced clinical study coordinator can be a rewarding and fulfilling career path with opportunities for growth, job security, and competitive compensation.

What are typical responsibilities of an advanced clinical study coordinator?

The responsibilities of an advanced clinical study coordinator can vary depending on the organization and the specific clinical trial or study they are working on. However, here are some typical responsibilities you might expect in this role:

  • Participant recruitment and enrollment: Developing and implementing strategies to recruit and enroll study participants, including advertising, outreach, and communication with potential participants.
  • Data collection and management: Overseeing the collection and management of study data, including ensuring that data is accurate, complete, and entered into study databases in a timely manner.
  • Participant communication: Communicating with study participants to provide information about the study, answer questions, and ensure that they are fully informed and comfortable with the study procedures.
  • Compliance and regulatory oversight: Ensuring that all study procedures are conducted in compliance with regulatory requirements and ethical guidelines, including obtaining informed consent from participants and reporting adverse events.
  • Study coordination: Coordinating study activities with other members of the study team, including principal investigators, research nurses, and other study coordinators.
  • Budget and resource management: Managing the study budget and resources, including tracking expenses, coordinating with vendors, and ensuring that the study is conducted within budget.
  • Quality control and assurance: Conducting regular quality control checks to ensure that the study is conducted according to protocol, and implementing corrective action as needed.
  • Documentation and reporting: Preparing study reports, including progress reports, safety reports, and final study reports, and ensuring that all documentation is complete and accurate.

 

Overall, the role of an advanced clinical study coordinator is to manage and coordinate all aspects of clinical studies, from study planning and design to study closeout. Effective coordination and communication with all stakeholders involved in the study, including study participants, principal investigators, and regulatory agencies, is essential to ensure the success of the study.

IS THIS THE BEST OPTION FOR ME?

To become an advanced clinical study coordinator, it’s typically necessary to have a background in a health-related field, such as nursing, pharmacy, or healthcare administration. Here are some of the qualifications and skills that are often required or preferred for this role:

  • Education: Many advanced clinical study coordinator positions require at least a bachelor’s degree, and some may require a master’s degree in a health-related field. 
  • Experience: Previous experience in clinical research, healthcare administration, or a related field is typically preferred for advanced clinical study coordinator positions. This could include experience working as a clinical research coordinator or research assistant, or experience in healthcare project management.
  • Knowledge of regulations: Advanced clinical study coordinators must have a thorough understanding of the regulatory requirements for clinical research, including FDA regulations and International Conference on Harmonization (ICH) guidelines.
  • Organizational skills: Advanced clinical study coordinators are responsible for coordinating multiple aspects of clinical studies, including scheduling study visits, tracking participant data, and ensuring that all study activities are conducted according to protocol. Strong organizational skills and attention to detail are critical for success in this role.
  • Communication skills: Advanced clinical study coordinators must be able to communicate effectively with a wide range of stakeholders, including study participants, principal investigators, study sponsors, and regulatory agencies. This requires strong written and verbal communication skills.
  • Critical thinking and problem-solving: Advanced clinical study coordinators must be able to think critically and troubleshoot issues that arise during the course of a clinical study. They must be able to identify problems and implement solutions to keep the study on track and ensure participant safety.

 

Overall, a combination of education, experience, and specialized skills is required to become an advanced clinical study coordinator. However, there are many different pathways to this career, and some employers may have specific requirements or preferences depending on the type of studies they are conducting.

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.

NEW JOBS POSTED TODAY

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.

[viares_jobs-table-course filter=”study Coordinator”]

clinical research online course - clinical study coordinator

Advanced Training Modules + VIARES Study Guide + Certification Exams. Lifetime Access to Unmatched Curriculum:

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80 contact hours, 8.0 CEUs
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Clinical Research Associate Certification Tuition

Accredited and Industry-recognized certification with unmatched curriculum. Seminars, assignments and exams tailored to your need to stay ahead and stand out for the new job role! Increase salary potential by €52 EUR-80k+. 100% Money-back Guarantee with 5 Day Refund Policy.

Original price was: $ 93.90.Current price is: $ 74.90.
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Clinical Study Coordinator II
Original price was: $ 93.90.Current price is: $ 74.90.
one payment •  life-time access
SINGLE COURSE DEAL
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  • LIFE-TIME access to this course
  • VIARES Certificates (industry recognized)
  • Clinical Research Library
  • Community & updates
  • Free access to the Job-Hub
  • 5-day money-back guarantee
  • Downloadable resources
  • Career Accelerator Program

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Original price was: $ 1,349.90.Current price is: $ 224.90.
all courses •  life-time access
BEST DEAL
  • LIFE-TIME access to all of our courses
  • VIARES Certificates (industry recognized)
  • Clinical Research Library
  • Community & updates
  • Free access to the Job-Hub
  • 5-day money-back guarantee
  • Downloadable resources
  • Career Accelerator Program
  • Clinical Research Virtual Lab
  • Academy Priority Support
VIARES Academy
store rating5.00 / 5
product rating4.87 / 5
302 reviews
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5 Day Money-back Guarantee!

We pride ourselves on high-quality programs. That’s why we offer a 5-day no-questions-asked 100% money-back guarantee. If for any reason you are unhappy, you will get a full refund.

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What VIARES members get

Your membership to VIARES includes everything you need to excel in your clinical research career.

Worldwide LinkedIn community

Connect with peers worldwide to share insights, best practices, and engage in thought-provoking discussions.

Comprehensive Resource Library

Access a vast collection of templates, tools, and playbooks to enhance your clinical research work.
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Career center

Redefine your career trajectory and fast-track your personal growth with powerful career mapping and feedback tools.

Easy Learning Portal

Enjoy a user-friendly platform that makes accessing course materials and resources straightforward and convenient.
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Accredited Courses

Develop the latest and most in-demand clinical research skills with 100% online and globally recognized courses.

 

VIARES is known by the world’s leading organizations for for clinical reasearch providing you with the best training for your future dream job!

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Job Support

With VIARES you also get support with finding your clinical research dream job.

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VIARES’ digital certificates are a proven way to showcase that you mastered a new skill and upgrade your resume to land your next dream job.

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What alumni say about this program

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4.9
Based on 300 reviews
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Nay G.
Nay G.
Verified ownerVerified owner
5/5

the course was amazing. well tailored and knowledgeable expertise.

7 days ago
Amy Staton
Amy Staton
Verified ownerVerified owner
3/5

I'm pleased with the package, but my assignments are not being graded. The issue must be resolved before I purchase any additional courses.

1 week ago
Susan S.
Susan S.
Verified ownerVerified owner
4/5

Great basic understanding of the TMF process, but more content on creating/preparing and the closeout processes would be helpful.

2 weeks ago
Anonymous
Anonymous
Verified ownerVerified owner
4/5

Very informative but the payment automatically came off my account before I could apply my discount code so that was a little disappointing. Once I finish I can say more

2 months ago
Samuel
Samuel
Verified ownerVerified owner
4/5

course content very good ( i give it 105%) .Just a few typos which is not a deal breaker

2 months ago
MALICK DIOUF
MALICK DIOUF
Verified ownerVerified owner
5/5

great and compact courses

5 months ago
Alungile Ntsika Fileyo
Alungile Ntsika Fileyo
Verified ownerVerified owner
5/5

Great 👍 and relevant information

5 months ago
Anonymous
Anonymous
Verified ownerVerified owner
3/5
5 months ago
Namugera Mariam
Namugera Mariam
Verified ownerVerified owner
5/5

It has been apleasure

5 months ago

Related Clinical Research Programs

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PATRICIA HOLLIS

in the industry for 21 years

Patricia has been in the clinical research industry for over 20 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.

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  • Online access to our learning management system

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