Advarra Careers is hiring for the position of Advarra Research Associate I in Bengaluru, India. This hybrid opportunity is ideal for candidates with experience in clinical research coordination, pharmacovigilance, clinical data management, or records management.
Candidates with knowledge of clinical trial protocols, GCP guidelines, and clinical research operations can apply for this exciting clinical research job opportunity in Bengaluru.
Author: Pharmabharat Editorial Team
Published Date: May 22, 2026
About Advarra
Advarra Official Website is a global leader in clinical research technology and ethical review solutions. The company supports sponsors, CROs, sites, and patients by streamlining clinical trial operations and accelerating research innovation.
Advarra focuses on building connected clinical research ecosystems through advanced technology platforms, ethical review services, and operational expertise.
Job Overview
| Details | Information |
|---|---|
| Job Role | Research Associate I |
| Company | Advarra |
| Job Location | Bengaluru |
| Job Type | Full-Time |
| Work Mode | Hybrid |
| Experience | 6 Months โ 1 Year |
| Industry | Clinical Research |
| Department | Clinical Operations / Research |
| Posted Date | May 22, 2026 |
Key Responsibilities
The selected candidate will work closely with clinical trial teams and reporting managers to support study setup and documentation activities.
Major Responsibilities Include:
- Interpret clinical trial protocols and design study calendars
- Develop and manage clinical trial site budgets
- Design and develop case report forms (CRFs)
- Utilize Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) systems
- Track assignments using internal case management tools
- Participate in protocol discussions and team meetings
- Ensure quality standards for clinical research documentation and workflows
Eligibility Criteria
Basic Qualifications
Candidates should possess:
- Knowledge of clinical research methodology
- Understanding of Good Clinical Practice (GCP) guidelines
- Familiarity with industry regulations related to human research
- Strong organizational and administrative skills
- Proficiency in Microsoft Office and business software
- Ability to work independently and within teams
Preferred Experience
Applicants with 6 months to 1 year of experience in the following areas are preferred:
- Clinical Trial Coordination
- Clinical Data Management
- Pharmacovigilance
- Records Management
Skills Required
- Clinical protocol interpretation
- Clinical trial documentation
- Budget development
- EDC and CTMS exposure
- Communication and collaboration skills
- Attention to detail
- Time management
Salary Expectations
Based on current clinical research industry standards in India, the estimated salary for the Research Associate I role at Advarra ranges between:
โน3.8 LPA โ โน5.8 LPA
Actual compensation may vary depending on experience, skills, and interview performance.
Why Join Advarra?
Working at Advarra offers candidates exposure to global clinical research operations and innovative healthcare technology solutions.
Benefits May Include:
- Hybrid working opportunity
- Exposure to global clinical trials
- Collaborative work culture
- Career growth in clinical research
- Training and skill development
- Inclusive and employee-focused environment
How to Apply
