Advarra Hiring Research Associate I | Clinical Research Jobs 2026
Advarra is hiring Research Associate I professionals for its clinical research and clinical operations team in Bengaluru.
This opportunity is ideal for candidates interested in Clinical Research, Clinical Trial Coordination, Pharmacovigilance, Clinical Data Management, CTMS, EDC Systems, and Clinical Operations careers.
📋 Advarra Hiring Overview
- Company: Advarra
- Role: Research Associate I
- Location: Bengaluru
- Work Mode: Hybrid
- Department: Clinical Operations / Research
- Industry: Clinical Research
- Experience: 6 Months – 1 Year
- Employment Type: Full-Time
🏢 About Advarra
Advarra is a global leader in clinical research technology and ethical review solutions supporting sponsors, CROs, research sites, and healthcare organizations worldwide.
The company focuses on accelerating clinical trials through innovative technology platforms, ethical review services, and connected clinical research ecosystems.
📌 Key Responsibilities
- Interpret clinical trial protocols and study requirements
- Design and manage study calendars
- Develop and maintain clinical trial site budgets
- Create and manage Case Report Forms (CRFs)
- Work with CTMS and EDC systems
- Track assignments using internal management tools
- Participate in protocol discussions and study meetings
- Ensure quality standards in clinical documentation
- Support clinical operations workflows and reporting
🎓 Eligibility Criteria
Eligible Qualifications
- B.Pharm / M.Pharm / Pharm.D
- BSc / MSc Life Sciences
- Clinical Research & Healthcare Related Degrees
🧑💻 Experience Required
- 6 Months – 1 Year Preferred
- Clinical Trial Coordination Experience
- Clinical Data Management Exposure
- Pharmacovigilance or Records Management Experience
⭐ Required Skills
- Clinical protocol interpretation
- Knowledge of GCP guidelines
- CTMS & EDC system exposure
- Clinical trial documentation knowledge
- Communication and collaboration skills
- Strong organizational abilities
- Time management and attention to detail
🌍 Benefits of Working at Advarra
- Hybrid working opportunity
- Exposure to global clinical trials
- Career growth in clinical research
- Collaborative work environment
- Training and professional development
- Employee-focused work culture
🚀 Why This Role is Valuable
This Research Associate I role provides excellent opportunities to build expertise in:
- Clinical Research Operations
- Clinical Trial Coordination
- Clinical Data Management
- CTMS & EDC Systems
- Clinical Documentation
- Regulatory Compliance & GCP
Candidates will gain exposure to global clinical trial operations, protocol management, and clinical research technology systems.
📄 Resume & Interview Tips
- Highlight clinical research or CDM experience clearly
- Mention CTMS, EDC, or CRF exposure if available
- Showcase GCP and protocol understanding
- Add internships, projects, or research experience
- Keep resume ATS-friendly and concise
🚀 Job Application Link
Please make sure to read the complete job description carefully before submitting your application. Understanding Clinical Research workflows, GCP guidelines, CTMS, and EDC systems improves your chances of selection and creates a strong professional impression.
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