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Qtech-Sol Professional Development Center

Advanced Clinical Research Associate (ACRA)


Advanced Clinical Research Associate (ACRA)

3 Students Enrolled
06 Weeks / 175 Hours

The course provides a thorough Foundation, Advanced and Project Management related concepts focusing clinical trials, drug development, Study design, Project Management, and Monitoring concepts of Clinical Sciences in reference to roles and responsibilities performed by Clinical Research Associate. The concepts include a protocol development, assessment and reporting of adverse events and explains GCP-ICH guidelines along with other necessary regulatory information. The course emphasizes on understanding of the science and the expectations of initiating, conducting, monitoring, and managing clinical trial related work. This training will develop the technical skills and knowledge pertaining to roles and responsibilities of CRA – In House. Students will get exposure to real time practices pertaining to Case Report forms (CRFs), Trial Master File (TMF), Clinical Trial Protocol, Clinical Trial Budget, and Audit. The course curriculum is designed to give an edge to obtain job opportunity in clinical research field.

Our Programs are delivered in 3 Different ways for convenience of student:
• Self-Paced Individual Program (SIP)
– Skill and Job Oriented Certificate programs, delivered as Self-Paced Online with project solutions
• Self-Paced Blended Program (SBP)
– Skill and Job Oriented Certificate programs, delivered as Self-Paced Online with project solutions. Support thru Email and Phone for queries. Student participates in 7 days Post Training Assistance program for Resume preperation
• Self-Paced Package Program (SPP)
– Skill and Job Oriented Certificate programs, delivered as Self-Paced Online with project solutions. Support thru Email and Phone for queries. Student participates in 15 days Post Training Assistance program for Resume preperation, Interview Narratives and Mock session. Obtains Job refferal and leads for application with clients and vendors

Lessons: 15 Lessons Duration: 06 Weeks / 175 Hours Language: English
Admission Requirements:

Recommended: An Associate or Bachelor’s degree in Medicine, Nursing, Pharmacy, Public health Biology, Biochemistry, Biotechnology, Chemistry, Clinical Research, Biomedical engineering, Public health, Pharmacology, or toxicology, Medical Device & Technology, Psychology, Sociology and Healthcare Administration.


Institutional Scholarship / Promotion is available for selected on tuition. We review your education background, certifications, and prior experiences (if applicable), to evaluate your eligibility. Qualified student will be provided with the promo code for scholarship on Tuition.
Please Email your resume to Human Resources hrs@qtech-solutions.com to check on your eligibility. We will contact you. Q-tech’s objective is to provide you the right career pathway and advancement required to meet your career goals.

Learning Outcomes:

The Benefit Student Gains

1) Upgrading the Knowledge required.
2) Better Resume Placement for promising jobs.
3) Low Investment, high learnings
4) Learn from Anywhere, Anytime at your pace.
5) Job and Title Based Tasks as followed and Practiced in industry
6) Applying Concept into Real-time (Policies, governance and tools)
7) Work on Role Based Tasks followed and Practiced in industry
8) Mocks and Narratives for Client Discussions
9) Readiness to work with limited support

Career Pathways

Our objective is to help students to meet the following career pathways. Typical Clinical Research Associate (CRA) Job Titles the candidates can apply after this training program are :

Clinical Research AssociateClinical Program Manager
Clinical Research CoordinatorClinical Trial Assistant
Clinical Research SpecialistTrial Regulatory Coordinator
Clinical Research ManagerResearch Admin Assistant
Research RN CoordinatorClinical Project Manager
Research NurseTrial Master File (TMF)
Clinical Study ManagerClinical Trial Management Associate
Documentation SpecialistAdministrative Associate
  • Curriculum Overview:

    Program is designed by industry experts meeting job and title-based learnings needed for students and young professionals to get into jobs. The training provides in depth knowledge of roles and responsibilities of Clinical Research Manager. The curriculum includes 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. Clinical Trial Budget

    2. Investigator Selection

    3. Pre-Study Visit

    4. Protocol

    5. Informed Consent Preparation

    6. Investigational New Drug (IND)


    7. Institutional Review Board (IRB)

    Regulatory Correspondence

    8. Case Report Form (CRF)

    9. Site Monitoring

    10. Co-Monitoring Visits

    11. Study Initiation Visit

    12. Clinical Trial Management Systems

    (CTMS) Tracking Recording

    13. Trial Master File

    14. Database Lock

    15. Audit

    What is the difference between
    Basic CRA and Advanced CRA?

    CRA Basic and core topics and exercises Certain educational background isstronglyrecommended to enter the industry Designed for non-experienced individuals to enter into field In depth knowledge of roles and responsibilities of CRA Plus, theoretical aspect with projects which help to understand industry requirements

    ACRA Advancedtopics and exercises Prior training or relevant experience is required Designed forexperienced professionals to add new skills set Exposure to diverse CRA exercises, real time documentation + advanced learning supported by practical case scenario tasks and follow up process




5.00 average based on 3 ratings

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  • "I am very thankful to Qtech learning center team for providing training in Clinical Research Project Management (AACR), as it will be helpful for me to gain experience in real time.

    Maureen D

    Paul A

  • The training helped me enhance my skills. The training was given in a very well planned, organized and professional manner


    Neepa Y

  • The program was extremely helpful, and the instructions were very knowledgeable. Thank you very much.


    Lily W

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