Advarra is hiring for 2 clinical research roles in Bengaluru, India: Research Associate I and Coverage Analyst II. Both positions are full-time and hybrid, offering opportunities for professionals with backgrounds in clinical research, clinical data management, pharmacovigilance, clinical trial coordination, medical writing, and related life-sciences domains.

These Advarra jobs in Bengaluru involve working with clinical trial protocols, study documentation, clinical trial management systems (CTMS), electronic data capture (EDC), budgets, case report forms, and coverage analysis.

Advarra Hiring 2026 – Job Overview

1. Advarra Research Associate I – Bengaluru

The Research Associate I role focuses on supporting clinical trial study setup and documentation. The position requires candidates to understand clinical trial protocols and use clinical research technology to develop calendars, budgets, financials, and case report forms.

Research Associate I Responsibilities

The selected candidate will be responsible for:

• Interpreting clinical trial study protocols to design and develop study calendars.
• Reviewing clinical trial agreements and sponsor budgets to develop site budgets.
• Designing and developing case report forms (CRFs).
• Learning and using Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) systems.
• Supporting the development of calendars, budgets, financials, and case report forms.
• Completing daily and weekly assignments according to established quality criteria.
• Using internal case-management and reporting software to track assignments.
• Participating in team meetings and contributing to discussions involving customer cases and clinical trial protocols.

Research Associate I Qualifications

Candidates should have:

• Knowledge of clinical research methodology.
• Understanding of industry regulations and Good Clinical Practice (GCP).
• Ability to work independently and collaboratively.
• Good organizational and administrative skills.
• Familiarity with Microsoft Office and business software.

Preferred Experience

Advarra prefers candidates with 6 months to 1 year of experience in areas such as:

• Clinical Trial Coordinator
• Clinical Data Management
• Pharmacovigilance
• Records Management

2. Advarra Coverage Analyst II – Bengaluru

The Coverage Analyst II position focuses on clinical trial coverage analysis and determining how medical procedures and services associated with clinical research studies should be categorized for billing purposes.

The role requires candidates to interpret study protocols, informed consent forms, clinical trial agreements, regulations, clinical guidelines, and institutional policies.

Coverage Analyst II Responsibilities

Key responsibilities include:

• Reviewing clinical research protocols and informed consent forms.
• Reviewing Clinical Trial Agreements and other study-related documentation.
• Creating coverage analyses and billing guides.
• Determining whether clinical research studies qualify under applicable Medicare Clinical Trial Policy requirements.
• Identifying medical procedures and services that may qualify as routine costs or study-sponsored costs.
• Researching and applying applicable policies, regulations, guidance, and clinical guidelines.
• Applying Medicare regulations and institutional guidance to determine routine-care services.
• Completing daily and weekly coverage-analysis assignments.
• Documenting coverage analysis and associated information in clinical trial management systems.
• Using internal case-management and reporting software.
• Participating in customer-case and protocol discussions.
• Training and mentoring new team members.
• Identifying knowledge gaps and supporting continuous improvement initiatives.
• Developing internal knowledge-sharing documents and training materials.

Coverage Analyst II Qualifications

Applicants should have:

• A Bachelor’s or Master’s degree in science, preferably with a background in clinical research or a related domain.
• Sound knowledge of clinical research methodology.
• Knowledge of industry regulations and Good Clinical Practice (GCP).
• Strong organizational and administrative abilities.
• Ability to work independently and as part of a team.
• Familiarity with Microsoft Office and business software.

Preferred Experience

Advarra lists 2–3 years of experience in areas such as:

• Coverage Analysis
• Calendar and Budget Setup
• Clinical Trial Coordination
• Clinical Data Management
• Pharmacovigilance
• Medical Writing
• Medical Coding
• Related clinical research domains

Candidates should also have strong communication and customer-service skills, proficiency with Microsoft Word, Excel, and PowerPoint, and the ability to collaborate with internal and external stakeholders.

Why Consider Advarra Clinical Research Jobs?

These positions provide exposure to several important areas of clinical research operations, including:

• Clinical trial protocols
• CTMS and EDC platforms
• Clinical trial documentation
• Clinical data management
• Study budgets and financials
• Case report forms
• Coverage analysis
• Medicare clinical trial requirements
• GCP and clinical research regulations
• Clinical trial technology

For candidates looking to build experience across clinical research operations and technology-enabled clinical trial processes, these roles offer exposure to multiple functional areas.

How to Apply

Application Link For Research Associate I

Application Link For Coverage Analyst II