Advarra, a global leader in clinical research solutions and ethical review services, is currently hiring for the position of Research Associate I in Bengaluru, India. This is an excellent opportunity for freshers and early-career professionals (0โ1 year experience) in clinical research, clinical data management (CDM), and pharmacovigilance (PV).
If you are looking to build a career in clinical trials, EDC, CTMS, and protocol development, this role offers strong exposure to industry-standard tools and processes.
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Job Overview
- Role: Research Associate I
- Company: Advarra
- Location: Bengaluru, India (Hybrid)
- Experience: 0โ1 Year
- Job Type: Full-Time
- Date Posted: May 6, 2026
Key Responsibilities
- Interpret clinical trial protocols to design study calendars
- Develop site budgets using clinical trial agreements and sponsor inputs
- Design and develop Case Report Forms (CRFs)
- Work on Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC) platforms
- Ensure quality delivery of calendars, financials, and CRFs
- Track assignments using internal case management tools
- Collaborate with team members and reporting managers
- Participate in protocol and case discussions
Required Qualifications
- Knowledge of clinical research methodology, GCP (Good Clinical Practice), and regulatory guidelines
- Strong organizational and administrative skills
- Ability to work independently and in a team environment
- Proficiency in MS Office and business software
Preferred Qualifications
- 6 months to 1 year experience in:
- Clinical Trial Coordination
- Clinical Data Management (CDM)
- Pharmacovigilance (PV)
- Records Management
Skills & Competencies
- Attention to detail and accuracy
- Strong communication and comprehension skills
- Ability to manage multiple tasks efficiently
- Familiarity with clinical trial systems (EDC/CTMS)
Salary (Estimated)
- โน3.2 LPA โ โน5.5 LPA (INR)
(Based on industry standards for entry-level clinical research roles in India)
Why Join Advarra?
- Work with a global clinical research leader
- Exposure to end-to-end clinical trial processes
- Collaborative and patient-centric work culture
- Opportunity to work with cutting-edge clinical technologies
- Strong career growth in clinical research and data science
How to Apply
