Clinical Research Coordinator

Training and more

The VIARES Clinical Research Coordinator program is more than just training.

We aim to improve employability as Clinical Research Professionals for our participants. Our setup enables participants to complete their program next to a full-time job or in a focused effort. On successful completion of this program graduates will have acquired knowledge, skills and competencies to start at an entry level role as Clinical Research Coordinator or similar.

Enjoy all our services during your program enrollment. 

  • modules including
    • e-learnings
    • assignments
    • knowledge checks
  • VIARES ACADEMY certificate
  • GCP certification
  • Talent Profile to connect you with open jobs
  • Talent Days to connect with our industry partners and learn about career opportunities
  • Talent Portal to apply for posted jobs available to the Talent Program Community
  • modules including
    • e-learnings
    • assignments
    • knowledge checks
    • pre-recorded webinars
  • VIARES ACADEMY certificate
  • GCP certification

Program

The Clinical Research Coordinator program consists of the Clinical Research Fundamentals Program and five consecutive modules. You will complete the following learning activities:

  • review the e-learning
  • submit the assignment
  • watch the pre-recorded webinar and join live instructor-led webinars
  • take the module test
  • take the final exam

Successfully complete all activities to obtain your VIARES ACADEMY certificate.

As pre-requisite, please complete the Clinical Research Fundamentals Program before starting this program.

Learning Elements:

  • Understand the role of the CRC as member of the clinical study team and typical activities of the CRC related to:
  • Protocol review and clinical trial feasibility
  • Managing clinical trial subjects from start to finish
  • Preparing for monitoring visits
  • Managing Essential Documents
  • Handling Investigational Medicinal Product
  • CRF completion & Data Management
  • Interaction with IRBs/IECs

Next Live Webinar Dates

2019: October 2019 Dates to be announced

All webinars start 11am EST and are set for 60 minutes. You can take as many webinars as you like.

Learning Elements:

  • Understand the activities and responsibilities of the CRC whilst planning for an upcoming study.
  • Typical activities involved in preparing for a clinical study:
    • Reviewing clinical trial documents (e.g. protocol, ICF, 1572 etc.)
    • Planning for staff and site facilities
    • Preparing IRBs/IECs submission
    • Undertaking feasibility
    • Clinical Trial Agreement

Next Live Webinar Dates

2019: October 2019 Dates to be announced

All webinars start 11am EST and are set for 60 minutes. You can take as many webinars as you like.

Learning Elements:

  • Understand the activities involved in managing a clinical trial from the study initiation to the study close out.
  • Understand how to efficiently and effectively conduct and coordinate the clinical trial at the site.

Next Live Webinar Dates

2019: October 2019 Dates to be announced

All webinars start 11am EST and are set for 60 minutes. You can take as many webinars as you like.

Learning Elements:

  • Understand the challenge of subject recruitment and retention in clinical trials.
  • Understand the subject’s perspective of participating in clinical trials.
  • Be aware of key strategies for subject recruitment and retention in clinical trials.

Next Live Webinar Dates

2019: October 2019 Dates to be announced

All webinars start 11am EST and are set for 60 minutes. You can take as many webinars as you like.

Learning Elements:

  • Understand the risks arising in a clinical trial.
  • Understand the risk management process.
  • Understand how to priorities risks.
  • Understand how to develop a risk management plan specific of a clinical trial.

Next Live Webinar Dates

2019: October 2019 Dates to be announced

All webinars start 11am EST and are set for 60 minutes. You can take as many webinars as you like.

Program Dates​

You can start your program after enrollment. We recommend to join one of the regular information webinars, where we provide guidance and tips on how to best take the program.

Enrollment

until August 12, 2020

first come – first serve

Program LIVE WEBINARS

DAY

TIME

Kick-Off Webinar

August 13, 2020

START: 5:30 pm CET

END: 6:30 pm CET

BLOCK 1

Roles and Responsibilities of the CRC

Preparing for a clinical study

Managing a study

August 22, 2020

START: 3:00 pm CET

END: 6:00 pm CET 

BLOCK 2

Subject Recruitment and Retention

Managing risks in clinical trials

September 05, 2020

START: 3:00 pm CET

END: 5:00 pm CET 

Information can be subject to change without notice.

Expert instructors​

Eric Klaver
Gabriele Disselhoff

Who should attend

This academy will be of benefit to anyone aiming to start a career as Clinical Research Professional. If you have

  • a university degree in life sciences or natural sciences, or
  • related clinical research or study site work experience
    • i.e. Clinical Trial Assistants, Project Associate, Data Specialist, TMF Coordinator, Study Nurse, or similar roles.

you will get the most out of it.

Is this academy right for me? We are happy to help you make the right decision. Email us at academy@viares.at.

Typical jobs with this skills

You could apply for jobs like:

  • Clinical Research Coordinator
  • Clinical Trials Coordinator
  • Clinical Site Coordinator or similar 

Affordable and flexible

  • Our Talent Programs come at very affordable cost wherever you are in your career.
  • Choose from multiple payment options to adjust to your personal preferred payment schedule.
  • Invite your friends with your personal discount code to sign up and get refunded.

Flexible Plans

Our plans have two things in common – they cover your individual needs and are affordable.

Not yet ready to invest in your career? Sign up to our email list and we’ll keep you updated about our upcoming academy dates!

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Clinical Research Coordinator

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Related Academy Programs

Clinical Research Fundamentals

Acquire basic knowledge about medicines development and Clinical Research. Includes GCP certificate.

Clinical Trial Assistant

Understand the role of the CTA in the wider project team to ensure clinical trial success.

Site Contract Specialist

Understand the key aspects of clinical trial agreements and related budget and payment processes.

Study Start Up Specialist

Understand the responsibilities and involvement in the project life-cycle, core submission documents and processes.

Clinical Research Data Science

Learn about data-driven research process and gain confidence in the ethics, curation, analysis, and presentation of data.