Advanced Clinical Research Associate (ACRA)


Advanced Clinical Research Associate (ACRA)

1 Student Enrolled

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 2 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.

Category: Clinical Research Lessons: 15 Lessons Duration: 04 Weeks / 120 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:

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 to check on your eligibility. We will contact you. Qtech'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 Associate Clinical Program Manager
Clinical Research Coordinator Clinical Trial Assistant
Clinical Research Specialist Trial Regulatory Coordinator
Clinical Research Manager Research Admin Assistant
Research RN Coordinator Clinical Project Manager
Research Nurse Trial Master File (TMF)
Clinical Study Manager Clinical Trial Management Associate
Documentation Specialist Administrative 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



    The real time scenario case is assigned to each topic:

    1. Clinical Trial Budget

    2. Investigator Selection

    3. Pre-Study Visit

    4. Protocol

    5. Informed Consent Preparation

    6. Investigational New Drug (IND) Application

    7. Institutional Review Board (IRB)

    8. Case Report Form (CRF)

    9. Site Monitoring

    10. Co-Monitoring Visits

    11. Study Initiation Visit

    12. Clinical Trial Management Systems (CTMS)

    13. Trial Master File

    14. Database Lock

    15. Audit

    What is the difference between
    Basic CRA and Advanced CRA?


    Basic and core topics and exercises

    Certain educational background is strongly recommended to enter the industry

    Designed for non-experienced individuals to enter into field

    In depth knowledge of roles and responsibilities of CRA + theoretical aspect with projects which help to understand industry requirements


    Advanced topics and exercises

    Prior training or relevant experience is required

    Designed for experienced 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




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  • maureen

    - Marissa Sisson

    It was self-paced and easy to understand. Due to its self-paced format, I was able to make this program fit well with my school's requirements for the internship. The information was also very interesting, and I enjoyed the material. I think it will help me in my future career endeavors. This course was very informational and interesting. I believe that coming straight out of this program will leave me with a solid base of knowledge and the confidence needed to begin a career as CRA.

    - Gamal Aldaghady

    It was very interesting CRA training course. Topic, professional presentation, Quiz and test, makes the difference between a good training session and a GREAT training session. I like the competent materials course

    - Keisha Felix

    I highly recommend the CRA training course with Q-tech Solutions, Inc. It covers various areas of knowledge needed to succeed as a CRA within the industry. Prior to completing the training course, I had limited knowledge and experience within the clinical research field. After completing the course, it expanded my knowledge of the CRA role and helped me talk more confidently during my interviews. Within six months of completing the program, I was offered a position with one of the top CROs within the industry. Thanks, Q-tech!