PLANNING FOR CLINICAL TRIALS AND TRACKING
Qtech-Sol is a Clinical Science Training Provider. The training provides in depth knowledge about Role of a CRA for Clinical Trial Process Planning, 6-Months Planning ahead of Clinical Trial Kickoff, Study Initiation Process, Clinical Trial Budgeting, Adverse Event Data Reconciliation and Archiving process. An Ideal person must have bachelor’s degree in degree in life science or other health-related discipline to become a CRA or CRC. Few entry-level positions (CTA) require Associate or High school diploma. Qtech-Sol CRA Coursework is not wet lab experience, these are computer related roles performed using clinical data and tools, to support the progress of clinical trials being conducted. Person must have basic computer knowledge and works with Microsoft Word, Excel, Notepad, PowerPoint etc. The ideal person works within pharmaceutical or at hospital and research centers.
A Clinical Research Associate (CRA) manages clinical trials and studies related to pharmaceutical and biotechnological products, drugs, and procedures. They oversee recruiting study participants, collecting patient data, creating study documentation and conducting quality assurance audits to ensure study protocols are in order.
(Role based Lessons – Case Scenarios, Job Tasks with Solutions)
Each Lesson contains various delivery modes as presentation with voice over, course reading material (chapters), Quizzes for Practice (15 Set) and Test (10 Set), Short Questions, Role based Tasks (Exercises, along with solutions).
To complete your enrollment, please email your resume to email@example.com
An Associate or bachelor’s degree in life science or other health related. Few of the majors accepted for admission into this course are Medicine, Nursing, Pharmacy, Public health, Biology, Biochemistry, Biotechnology, Chemistry, Clinical Research, Biomedical engineering, Public health, Pharmacology, Toxicology and Healthcare Administration.
Qtech-Sol offers self-paced online courses. Student get started with the course when they are ready. They must complete the online application and pay applicable tuition. Student must submit their resume and copy of highest degree certificate obtained. These documents are used to validate the student’s name on certificate, contact information, course enrolled and their education eligibility to participate.
- Submit Online Application and email your resume.
- Pay applicable tuition (Shopping cart).
- Receive Course Activation email.
- Obtain access to Course and Solution bank (LMS).
- Receive support for subject related queries.
- Complete all lessons and Obtain Certificate of completion.
- Upgrading the Knowledge required.
- Better Resume Placement for promising jobs.
- Low Investment, high learnings
- Learn from Anywhere, anytime at your pace.
- Job and Title Based Tasks as followed and practiced in industry
- Applying Concept into Real-time (Policies, governance, and tools)
- Work on Role Based Tasks followed and practiced in industry
Your resume is front face to hiring recruiters and organizations to pre-screen or call for an interview. With competition out in market, does your resume meet the requirements. Contact us to participate in our Post Training Assistance (PTA)” program for resume build, interview narratives, and mock. It is as well important to know, the current hiring organizations in your area, open positions available, salary range, fitness of resume to apply and many more. During this PTA program you will have opportunity to discuss with our course specialist to learn and discover opportunities in small steps. We shall work together as team to achieve this goal.
Professional organizations and associations are membership-based groups comprised of people working in a similar field. They can be helpful resources for students to learn more about a field, develop connections and discover related opportunities.
Check out World-Wide Clinical Resource Information. Follow the resource links to learn what’s happening around the world on current news and updates about Clinical trials, Regulatory, CDM and Pharmacovigilance.
This course is designed by industry experts meeting job and title-based learnings needed for students and young professionals to get into jobs. The lessons below include theoretical and practical aspect of the role and tasks performed on day-to-day basis, along with exposure to various exercises per industry requirements
1. A 6 Month Process for planning Multinational Clinical Trials
2. Communication with Cross Functional Team
3. Selection of Investigation Site
4. Study Initiation
5. Clinical Trial Budget
6. Introduction to Adverse Event Reporting and Classification
7. Clinical Trial Budget – Advanced
8. Reconciliation and Archiving
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For additional information please call us on 732.770.4100 or ENQUIRE. One of our course specialists will contact you at earliest possible.