📘 Introduction
Qtech-Sol specializes in Clinical Science Training, offering a comprehensive program geared towards individuals aspiring to work as Clinical Research Associates (CRAs). Our course is meticulously structured to provide a strong foundation and practical skills necessary for these job roles. The program places a strong emphasis on the pivotal role of CRAs in various aspects of clinical research, including protocol design, site initiation, trial conduct, ongoing monitoring, and effective management of clinical trial data capture and audits. Our curriculum is strategically crafted to provide students with a competitive advantage in securing employment opportunities as CRAs within the pharmaceutical, biotechnology, medical device, clinical research organizations (CROs), and research clinic sectors.
🎓 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, real-world case studies, and a clear roadmap to job-ready success.
What you’ll get:
- Discover how our Clinical Research Associate (CRA) training prepares you for industry 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 – 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:
- Site Selection and Evaluation: Assess potential trial sites based on investigator qualifications, staff capabilities, infrastructure, and previous performance.
- Site Initiation and Training: Train site staff on protocol, GCP, SOPs, and regulatory procedures prior to trial commencement.
- Subject Recruitment & Informed Consent: Monitor enrollment and ensure informed consent is obtained ethically and per regulation.
- Monitoring Visits: Verify CRF data vs. source, assess protocol compliance, safeguard subject welfare.
- Safety Monitoring: Track/report AEs & SAEs to ensure participant safety and compliance.
- Data Quality & Integrity: Review for accuracy and consistency; resolve discrepancies per SOPs.
- Regulatory Compliance: Ensure ICH-GCP, FDA/EMA, and local requirement adherence.
- Communication & Coordination: Liaise between sponsor and site to address operational issues.
- Report Writing: Prepare monitoring visit reports, deviations, and CAPA documentation.
- Problem-Solving: Address protocol deviations and operational challenges.
🧭 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
8 Weeks / 168 Hours (Self-Paced Access via Qtech’s AI-Driven LMS). Extensions available upon request.
💰 Tuition and Payment Methods
Tuition Fee:USD $1,044.12
- 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
- Clinical Research Associate (CRA)
- Clinical Trial Monitor
- Clinical Research Coordinator (CRC)
- Clinical Trial Assistant
- Clinical Study Associate
- Junior CRA / CRA Intern