Advarra is a global leader in clinical research, dedicated to advancing human health through ethical review services, innovative technology, and deep industry expertise. By aligning patients, sites, sponsors, and CROs, Advarra accelerates clinical trials to improve lives.
Why Work at Advarra?
✅ Patient-Centric & Ethical Culture
✅ Collaborative & Inclusive Workplace
✅ Cutting-Edge Clinical Trial Solutions
Detailed Job Description
Position: Research Analyst I
Location: Bengaluru, India (Hybrid)
Job Type: Full-Time
Experience: 0-2 years
Key Responsibilities
✔ Analyze clinical trial study documents to extract critical data.
✔ Work with Clinical Trial Management Software (CTMS) for study support.
✔ Collaborate with project managers & cross-functional teams to meet deadlines.
✔ Review and optimize existing clinical research content.
✔ Ensure compliance with ICH-GCP guidelines and industry standards.
✔ Participate in team meetings & problem-solving discussions.
Skills & Qualifications
Basic Requirements
- Knowledge of clinical research methodology & GCP guidelines.
- Familiarity with MS Office & business software.
- Strong organizational & communication skills.
Preferred Qualifications
- 0-2 years in clinical data management, pharmacovigilance, or site coordination.
- Detail-oriented & proactive mindset.
- Ability to work in a culturally diverse environment.
Benefits & Work Culture
🔹 Hybrid Work Model (Bengaluru-based)
🔹 Inclusive & Supportive Team Environment
🔹 Career Growth in Clinical Research
🔹 Competitive Salary & Benefits
How to Apply
