If you’re looking to build a strong career in clinical research, clinical trial operations, or clinical data management, the Research Associate II job at Advarra is one of the best opportunities in Bengaluru. Advarra is a global leader in ethical review, clinical trial technology, and research compliance, making it an ideal workplace for candidates who want hands-on exposure to CTMS, EDC, CRFs, and clinical trial budgeting.
This role is perfectly suited for experienced freshers and early-career professionals with 1+ years of clinical research experience, especially those aiming to grow in clinical trial startup, protocol interpretation, and site budget development.
About Advarra
Advarra is a world-renowned clinical research organization offering IRB/IEC services, advanced clinical trial software, and operational support. Known for its patient-centric approach, quality focus, and collaborative culture, Advarra connects sponsors, CROs, sites, and patients to streamline global clinical trials.
Key Responsibilities
As a Research Associate II, you will support clinical trial startup activities across multiple systems and protocols. Key duties include:
1. Protocol and Document Interpretation
- Interpret clinical trial study protocols to design study calendars.
- Analyze clinical trial agreements (CTAs) and sponsor budgets to prepare site-level budgets.
2. eClinical System Configuration
- Design and develop Case Report Forms (CRFs) based on study requirements.
- Work with Advarra’s CTMS & EDC systems to configure calendars, CRFs, budgets, and financials.
3. Workflow Management
- Track daily tasks through internal case management tools.
- Ensure all deliverables meet internal quality standards and timelines.
4. Collaboration & Reporting
- Work closely with the reporting manager for prioritization.
- Actively participate in team discussions for protocol requirements and troubleshooting.
Required Qualifications
Basic Requirements
- Minimum 1+ year of experience in clinical research or related domain
- Strong knowledge of:
- Clinical research methodology
- ICH-GCP guidelines
- Industry regulations
- Ability to manage tasks independently and in a team
- Proficiency in MS Office and business software
- Excellent organizational and communication skills
Preferred Experience
Candidates with any of the following will have an added advantage:
- Clinical Trial Coordinator (CTC) experience
- Clinical Data Management
- Pharmacovigilance
- Records management
Benefits
While not explicitly listed, similar roles at Advarra typically include:
- Competitive salary with growth opportunities
- Hybrid/remote work flexibility
- Training on CTMS, EDC, and advanced eClinical systems
- Collaborative and inclusive work culture
- Exposure to global clinical research standards
Job Location
Bengaluru, India (Hybrid or Remote Eligible)
Salary (Estimated Range in INR)
₹4,50,000 – ₹7,50,000 per annum
(Industry-aligned estimate for Research Associate II roles in India.)
How to Apply
