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.

We train and certify you

 

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

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.

Requirements

This program will be of benefit to anyone with a bachelor degree in life science degree and/or first 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.

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.

WHY GET A CERTIFICATION?

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.

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.

Position – click to go to jobCompanyLocationDate CreatedSourceTitleId (key)
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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.

You can start the training right away and complete it at your own pace. This training contains 100 hours of online material.

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

Get Certified & Job Ready

On successful completion of this program, you will be certified and will have acquired knowledge, skills and competencies to grow into an intermediate level role as Clinical Study Coordinator, Clinical Research Coordinator, or similar.

The VIARES Clinical Study Coordinator program is more than just a training. It’s a life-changer!

Certificates:

  • VIARES

 

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

Your expert instructors

Hear from our graduates

Dilay

Dilay

It was a pleasure to take part in the VIARES Clinical Research Talent Program. I gained so much knowledge and understanding of clinical research. I would recommend it to anyone who is interested in the field of clinical trials.Many thanks to Dietmar

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Eglhofer, the whole team and all amazing tutors for providing this informative and very-well organized program

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Francis

Francis

VIARES provided me with the formal training and skills that would allow me to achieve my career and personal goals. A chance to complete this course afforded me the opportunity to experience the clinical trial training from different experienced

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professionals, whilst providing me with exposure to the international arena of clinical research management and the global concerns while interacting with the multi-national specialists and students. I developed skills in report writing, clinical trial design, and data management among others. I would recommend the VIARES ACADEMY for anyone eager to set strong foundations in clinical research whilst remaining all rounded.

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Clinical Study Coordinator II
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      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.

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