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Hiring Research Associate I – Clinical Research & CDM Role
Advarra is hiring Research Associate I professionals for Clinical Research, Clinical Data Management (CDM), and protocol support activities in Bengaluru.
This is an excellent opportunity for freshers and early-career professionals looking to build careers in:
- Clinical Research
- Clinical Data Management (CDM)
- Clinical Trial Operations
- EDC & CTMS Systems
- Protocol & CRF Development
👉 Learn Clinical Research Careers: Clinical Research Career Guide
📘 Learn Clinical Data Management: Clinical Data vs Clinical SAS
🏢 About Advarra
Advarra is a globally recognized clinical research technology and ethical review organization supporting sponsors, CROs, research institutions, and healthcare organizations worldwide.
- Clinical trial technology solutions
- IRB & ethical review services
- Clinical research operations support
- EDC, CTMS & protocol management systems
📋 Job Overview
- Role: Research Associate I
- Company: Advarra
- Location: Bengaluru, India
- Work Mode: Hybrid
- Experience: 0–1 Year
- Employment Type: Full-Time
- Date Posted: May 6, 2026
- Salary: ₹3.2 – ₹5.5 LPA
📌 Key Responsibilities
🧪 Clinical Trial & Protocol Support
- Interpret clinical trial protocols
- Design study calendars & workflows
- Develop Case Report Forms (CRFs)
- Support protocol-based documentation activities
💻 EDC & CTMS Activities
- Work on CTMS & EDC platforms
- Maintain study-related data accuracy
- Track assignments using case management systems
- Ensure quality delivery of project outputs
📊 Financial & Study Support
- Develop site budgets using sponsor agreements
- Support financial and operational study activities
- Maintain timelines and reporting accuracy
🤝 Team Collaboration
- Coordinate with reporting managers & teams
- Participate in protocol discussions
- Support process improvement initiatives
📚 Learn CDISC Standards: CDISC SDTM & ADaM Guide
🎓 Qualifications & Eligibility
✅ Required Qualifications
- B.Pharm / M.Pharm / Pharm.D
- BSc / MSc Life Sciences
- Basic understanding of Clinical Research
- Knowledge of GCP guidelines
- MS Office proficiency
⭐ Preferred Experience
- 0–1 Year experience
- Clinical Data Management (CDM)
- Clinical Trial Coordination
- Pharmacovigilance (PV)
- Records Management
💡 Required Skills
- Attention to detail
- Strong communication skills
- Time management & multitasking
- Clinical documentation understanding
- EDC & CTMS familiarity
- Analytical & organizational skills
🧠 Practice Interview Questions: Clinical Data & Analyst Interview Prep
🎁 Why Join Advarra?
- Work with a global clinical research organization
- Exposure to clinical trial systems & technologies
- Strong learning & development environment
- Career growth in CDM, PV & Clinical Operations
- Collaborative & patient-focused culture
📈 Explore More Career Paths: Career Options After B.Pharm
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