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Clinical Research

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Work Setting: Clinical Research Organizations (CRO) & Hospitals
Experience Level: Entry / Postgraduate
Compensation Guide: BDT 40,000 - 65,000 (Entry) • BDT 85,000 - 170,000 (Mid/Senior)
Demand Outlook: High / Stable Growth

Manage clinical trials, bioequivalence studies, GCP compliance, patient safety monitoring, and trial documentation.

Detailed Role Overview

Clinical Research Associates (CRAs) coordinate Phase I to IV clinical trials and Bioequivalence (BE) studies. They ensure trial sites adhere strictly to ICH-GCP (Good Clinical Practice) guidelines, ethical review board requirements, and protocol monitoring procedures.

A Typical Day on the Job

“Auditing clinical source documents at trial sites, verifying informed consent forms, counting investigational drug accountability logs.”

Core Skills & Technical Competencies

✓ ICH-GCP Guidelines
✓ Bioequivalence Protocol Design
✓ eCRF (electronic Case Report Forms)
✓ Clinical Site Monitoring
✓ IRB/Ethics Committee Approvals

Possible Entry Points & Designations

Clinical Trial Assistant (CTA) Fresh Grad / Trainee
Junior Clinical Research Associate (CRA) Fresh Grad / Trainee
Clinical Data Coordinator Fresh Grad / Trainee

Recommended Preparation Strategy

→ Certify in GCP guidelines
→ Understand bioequivalence metrics (Cmax, AUC0-t, 90% confidence intervals)
→ Study ethics in human experimentation

Academic Requirements

  • ✓ B.Pharm / M.Pharm / Pharm.D / Clinical Pharmacology

Want to Enter Clinical Research?

Schedule a 1-on-1 session with a mentor currently leading this department.

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