📘 Introduction
Qtech-Sol’s Advanced Clinical Research Associate (ACRA) program is built for professionals aiming to step into senior CRA responsibilities across complex trials. Strengthen protocol leadership, advanced monitoring, risk management, cross-functional coordination, and inspection readiness—so you can drive compliance, safety, and data quality from start-up through closeout.
🎓 Education Eligibility
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, Public Health, or Allied Health.
- International graduates and career changers with relevant science backgrounds are also eligible.
🎯 Unlock Your Career Potential – Join Our Live Webinar!
🚀 Ready to take the next step in Clinical Research?
Our upcoming webinar is designed to give you insider insights, senior CRA case studies, and a clear roadmap to job-ready success.
What you’ll get:
- Discover how Advanced Clinical Research Associate (ACRA) training prepares you for senior roles.
- Learn about career pathways, tuition options, and Resume Marketing Services.
- Get your questions answered directly by our experts.
👉 Seats are limited – reserve your spot today and move closer to your dream career!
📌 Building Relevant Experience – Senior CRA Core Responsibilities
Clinical Research Associates (CRAs) play a critical role in the execution and oversight of clinical trials. Below is a breakdown of the key tasks and duties that form the backbone of a CRA's responsibilities:
- Protocol Mastery: Lead protocol review and ensure alignment with global regulations.
- Site Selection & Evaluation: Qualify sites for readiness, performance, and risk.
- Training & Leadership: Coach investigators and site teams on protocol, GCP, and SOPs.
- Advanced Monitoring: Verify data vs. source, trend deviations, escalate CAPA, ensure subject safety.
- Safety Oversight: Manage AE/SAE workflows and documentation quality.
- Regulatory & TMF: Drive submission accuracy, TMF completeness, and inspection readiness.
- Risk & Data Quality: Use KRIs to anticipate issues and resolve discrepancies proactively.
- Communication & Collaboration: Liaise across sponsor/CRO/vendors/sites to unblock progress.
- Closeout Excellence: Ensure documentation completeness and compliant site deactivation.
🧭 RMS Support (Post-Training)
Graduates of the CRA program can enroll in Qtech-Sol’s Resume Marketing Services (RMS) for career support:
- Resume building and interview coaching
- LinkedIn optimization and recruiter outreach
- Job application tracking and HR narratives
- 1-on-1 mentorship and job referrals (where applicable)
⏱ Duration
4 Weeks / 90 Hours (Self-Paced Access via Qtech’s AI-Driven LMS). Extensions available upon request.
💰 Tuition and Payment Methods
Tuition Fee:USD $818.12
- Credit/Debit Card (Visa or Mastercard)
- Bank Transfer (ACH/Wire)
- Installment Plan: 2–3 payments – 8% Discount
- Full Payment in Advance: Receive 18% Early-Bird Discount
📌 Apply Now
💼 Job Titles to Apply After Training
- Senior Clinical Research Associate (Senior CRA)
- Clinical Research Associate (CRA)
- Clinical Trial Monitor
- Clinical Study Manager (entry path)
- Clinical Research Coordinator (CRC)
- Clinical Trial Assistant