📢 For Latest Job Updates
📲 Join WhatsApp Channel
💼 Follow on LinkedIn
Hiring Freshers for Clinical Trial Operations
Advarra
Bangalore
0–1 Years
Clinical Operations
₹3–5 LPA
🏢 About Company
Advarra is a global leader in clinical research technology and ethical review services. The company supports clinical trials worldwide by ensuring patient safety, regulatory compliance, and high-quality data management.
📌 Job Overview
- Role: TEMP Research Consultant
- Location: Bengaluru (On-site)
- Experience: 0–1 Years (Freshers Eligible)
- Qualification: B.Pharm / M.Pharm / Life Sciences
- Salary: ₹3 – ₹5 LPA
🎯 Key Responsibilities
- Interpret clinical trial protocols and design study calendars
- Create site budgets based on clinical agreements
- Design Case Report Forms (CRFs)
- Work with CTMS & EDC systems
- Track project deliverables and timelines
- Support clinical trial operations and reporting
💻 Required Skills
- Knowledge of clinical research & GCP
- Understanding of CTMS, EDC, CRF
- MS Office proficiency
- Strong communication skills
- Attention to detail
🎁 Why Join Advarra?
- Global CRO exposure
- Hands-on clinical trial experience
- Strong career growth in clinical research
- Learning & mentorship-driven environment
🎯 Interview Preparation Tips
- Revise clinical trial phases & lifecycle
- Understand CRF, CTMS & EDC basics
- Prepare GCP guidelines
- Practice real-life scenario questions
Helpful Resources:
🚀 Job Application Link
🛡️ Clinical Trial Compliance & Oversight Guide:
Advarra's research review and compliance ecosystems demand absolute precision in executing trial tracking workflows. Before verifying your profile deployment on their UltiPro recruiting platform, optimize your resume to highlight concrete familiarity with Institutional Review Board (IRB) standards, human subject protection regulations, clinical data quality auditing, and clinical site operational tracking protocols.
Advarra's research review and compliance ecosystems demand absolute precision in executing trial tracking workflows. Before verifying your profile deployment on their UltiPro recruiting platform, optimize your resume to highlight concrete familiarity with Institutional Review Board (IRB) standards, human subject protection regulations, clinical data quality auditing, and clinical site operational tracking protocols.
.png)
