Clinical Research Training
Get started in the rewarding field of Clinical Research.
Video about Us!
Watch to learn more about our class now!
Are you frustrated with...
Your search for clinical research training has been time-consuming and unsuccessful?
What if you could...
- Learning would suddenly be fun again, because you receive real coaching and engage with real people who are honestly interested in clinical research?
- You'd never again feel like you're pointlessly putting hours into a course, but instead you see your knowledge row continuously with each module?
- You know exactly how to present your expertise and knowledge in Clinical Research so that you land your dream role?
Introducing... 3T Clinical Research
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10 weeks of structured learning in a variety of topics in clinical research with live coaching calls once a week
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Online Support and access to private clinical research student community
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Learn at your own pace - Start and stop as it is convenient for you. Pick up where you left off.
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Lecture utilizing video and recorded screenshots.
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Lifetime access to material and Coaching
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Course PDF Book
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Practice questions
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Course completion certificate
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Clinical Research Career coaching and interview prep
Learning Objectives
As a result of participating in this course, you will be able to:
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Describe the process of developing an investigational product.
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Examine FDA standards as well as the International Conference on Harmonization (ICH) Guideline for Good Clinical Practices (GCPs)
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Examine the roles and responsibilities of the clinical research team before, during, and after a clinical study
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Determine the Investigator's requirements for supervising clinical research.
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Discuss the importance of an Institutional Review Board (IRB) in the clinical trial process, as well as its makeup and responsibilities.
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Explain the meaning of a clinical protocol, informed consent, investigator's brochure, and necessary documentation in clinical trials.
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Define the process of informed consent and the components of an informed consent agreement.
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Explain the many sorts of Monitoring Visits, including the planning, activities, and monitoring visit follow-up.
Define terms relating to safety management, adverse event detection, and reporting requirements.
About Your Coach
Sadaf has first-hand experience with the struggles to become a clinical research professional as well as the challenges that are faced after landing that first role. She has built a successful career as a clinical research associate (CRA) in the medical device and ophthalmology fields by beginning at the bottom and working her way up.
Sadaf has over 15 years of expertise in pre-clinical and clinical research, including approximately 4 years of experience in clinical data administration. She is presently working as a senior CRA for one of the leading sponsor businesses in the market. Sadaf holds a Master of Business Administration degree in addition to her Bachelor of Science in Healthcare Management degree and her Master of Science in Management and Leadership degree. Additionally, she holds the PMP certification as well as the ACRAC accreditation.
Bonuses
Real world Templates
In our course, you will have access to dozens of real world templates used in the clinical research world
E-Book
A 200+ page workbook with all course materials will be available as soon as you begin your onboarding call with us.
Special Monthly Pricing
At this time, since we are enrolling a new cohort we have a special monthly price instead of a one-time fee.
3-Month Plan
$1267
PER MONTH
- 10 weeks of structured learning in a variety of topics in clinical research with live coaching calls once a week
- Online Support and access to private clinical research student community
- Learn at your own pace - Start and stop as it is convenient for you. Pick up where you left off.
- Lecture utilizing video and recorded screenshots.
- Lifetime access to material and Coaching
- Course PDF Book
- Practice questions
- Course completion certificate
- Clinical Research Career coaching and interview prep
