"Research Associate II at Advarra (Bengaluru): A Top Opportunity for Clinical Research Professionals in 2025-26 Apply Now"
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(Research Associate II at Advarra Job 2025-26) |
The clinical research industry in India is growing at a rapid pace, and Bengaluru continues to be the leading hub for global clinical trial operations. Among the top organizations shaping this growth, Advarra stands out as a trusted global leader in ethical review, research compliance, clinical trial technology, and eClinical solutions.
For candidates looking to build a future-ready career in clinical research, clinical trial startup, budgeting, CRF development, or data management, the Research Associate II role at Advarra is one of the most promising opportunities in 2025.
Whether you're an experienced fresher or a professional with 1+ years of clinical research exposure, this position offers an outstanding platform to work with CTMS, EDC, CRFs, study protocols, and site budget development—all critical skills needed for long-term success in the global research ecosystem.
About Advarra:-
Advarra is a well-established name in the global research community, trusted for its world-class IRB/IEC services, research compliance solutions, and advanced clinical trial technologies. The company collaborates closely with:
Sponsors
CROs
Hospitals and clinical sites
Academic research institutions
Technology partners
Their mission is driven by patient safety, data integrity, and simplifying clinical operations through smart, modern tools. Working with Advarra allows professionals to grow in a highly ethical, innovative, and technology-focused environment.
Job Overview: Research Associate II:-
The Research Associate II position at Advarra is designed for candidates who have foundational experience in clinical research and want to move into more specialized areas, like:
Protocol interpretation
CRF development
Clinical trial startup coordination
Budget and finance structuring
eClinical system configuration
This role focuses on supporting multiple clinical trials simultaneously, helping sponsors and research teams achieve a smooth and compliant study startup.
Key Responsibilities:-
1. Study Protocol Interpretation:
Analyze and interpret clinical trial protocols to create accurate study calendars.
Understand sponsor expectations and study objectives to support downstream operational tasks.
Review Clinical Trial Agreements (CTAs) and financial documents to prepare site budgets.
2. eClinical System Configuration:
Develop and customize Case Report Forms (CRFs) tailored to study requirements.
Configure Advarra’s CTMS and EDC platforms, mapping out calendars, budgets, and site-level workflows.
Ensure that all eClinical data structures meet quality guidelines and protocol expectations.
3. Workflow & Task Management:
Manage day-to-day activities using internal case management tools.
Prioritize tasks independently while ensuring all deadlines are met.
Maintain accuracy and quality across all assigned deliverables, adhering to industry standards.
4. Team Collaboration & Communication:
Work closely with reporting managers to understand priorities and timelines.
Participate in team discussions to clarify protocol requirements, troubleshoot issues, and share insights.
Communicate effectively with internal stakeholders to maintain workflow transparency.
Required Qualifications:-
Basic Eligibility:
Minimum 1+ years of experience in clinical research or a related field.
Strong understanding of:
Clinical research methodology
ICH-GCP guidelines
Industry regulatory expectations
Confident task management skills.
Good command of MS Office and documentation tools.
Excellent organizational, analytical, and communication abilities.
Preferred Experience (Added Advantage):
Candidates with experience in any of the following domains are strongly preferred:
Clinical Data Management
Clinical Trial Coordination (CTC)
Pharmacovigilance
Records and document management
eClinical systems (CTMS/EDC)
Why This Role Is Worth Considering:-
Though specific benefits may vary, roles at Advarra typically offer:
Competitive salary & career growth pathway
Hybrid/remote flexibility
Hands-on training in CTMS, EDC, and eClinical applications
Exposure to international clinical research standards
Supportive and knowledge-driven work culture
Being part of Advarra means being part of a global community committed to improving the future of clinical trials.
Job Location:-
Bengaluru, India
(Hybrid/Remote work options may be available depending on project requirements)
Estimated Salary Range:-
₹4,50,000 – ₹7,50,000 per year
(Based on typical industry packages for Research Associate II positions in India)
How to Apply:-
You can apply directly through the official portal:
Application Link:
https://recruiting.ultipro.com/ADV1023AVR/JobBoard/6051d363-03fe-4650-945e-f836306a8388/OpportunityDetail?opportunityId=641e0461-e3dc-4f65-882f-f06b3ee4e775
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