Advarra is hiring for three clinical research roles in Bengaluru, India: Research Associate I, Coverage Analyst II, and TEMP Research Consultant. The positions cover clinical trial protocol interpretation, coverage analysis, clinical trial management systems, study start-up activities, and related clinical research operations.

Job Details

Company: Advarra
Posted: October 8, 2026

1. Research Associate I

Responsibilities

• Interpret clinical trial study protocols to design and develop calendars.
• Interpret clinical trial agreements and sponsor budgets to develop site budgets.
• Design and develop case report forms for clinical trial protocols.
• Develop familiarity with Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software.
• Complete calendars, budgets, financials and/or case report forms according to predetermined quality criteria.
• Use internal case management and reporting software to track and complete assignments.
• Participate in team meetings and discussions related to customer cases and protocols.

Eligibility & Qualifications

• Knowledge of clinical research methodology, industry regulations and Good Clinical Practice (GCP) guidelines related to human research.
• Ability to work independently and in a team environment.
• Good organizational and administrative abilities.
• Familiarity with MS Office and business software.

Preferred Experience

6 months–1 year of experience in areas such as:

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

2. Coverage Analyst II

Responsibilities

• Interpret clinical research protocols, informed consent forms, clinical trial agreements and other study documents to create coverage analyses/billing guides.
• Determine which medical procedures/services are routine costs and which should be billed to the study sponsor.
• Determine whether proposed clinical research studies qualify under the Medicare Clinical Trial Policy (NCD 310.1).
• Designate medical procedures/services based on relevant regulations and determinations.
• Research and apply federal and state regulations, policies, guidance and guidelines.
• Apply clinical guidelines, Medicare regulations and institutional guidance to determine routine care services.
• Complete daily and weekly coverage analysis targets according to quality criteria.
• Document coverage analysis and related information in the clinical trials management system.
• Use internal case management and reporting software.
• Participate in team meetings and protocol-related discussions.
• Train and mentor new team members on coverage analysis processes, tools and quality expectations.
• Identify improvement opportunities, lead focused training sessions and develop internal knowledge-sharing documents.

Eligibility & Qualifications

• Bachelor’s or master’s degree in Science with a background in Clinical Research or a similar domain.
• Sound knowledge of clinical research methodology, industry regulations and GCP guidelines related to human research.
• Ability to work independently and in a team environment.
• Excellent organizational and administrative abilities.
• Familiarity with MS Office and business software.

Preferred Skills & Experience

• Excellent customer service skills.
• Flexibility with working hours to collaborate with internal and external stakeholders.
• Proactive approach to identifying improvement opportunities.
• Excellent written and verbal communication skills.
• Solution-oriented approach to customer support.
• Proficiency in Microsoft Word, Excel and PowerPoint.

Preferred experience: 2–3 years in areas such as:

• Coverage Analysis
• Calendar and Budget Set-up
• Clinical Trial Coordinator at Site
• Clinical Data Management
• Pharmacovigilance
• Medical Writing
• Medical Coding
• Other relevant domains

3. TEMP Research Consultant

Responsibilities

• Develop familiarity with Advarra’s CTMS, Institutional Review Board (IRB) and CIRBI platforms.
• Support Client Services teams in functions including Translation Management, Safety Reporting, Ongoing Reviews, Site Termination and IRB submissions.
• Document issues and customer responses.
• Use software effectively to support high turnaround of Study Start-Up.
• Monitor customer escalations and support timely resolution.
• Complete assigned daily and weekly tasks according to quality and productivity metrics.
• Use internal case management and reporting software to track assignments.
• Participate in team meetings and discussions related to customer cases and protocols.

Eligibility & Qualifications

• Knowledge of clinical research methodology, industry regulations, study start-up activities and GCP guidelines related to human research.
• Ability to work independently and in a team environment.
• Good organizational and administrative abilities.
• Familiarity with MS Office and business software.

Preferred Experience & Skills

0–1 year internship experience in areas such as:

• Clinical Trial Coordinator at Site
• Study Start-Up
• Regulatory Affairs
• IRB and Ethics Committee Submissions
• Clinical Data Management
• Records Management

Additional preferred qualities include:

• Highly personable nature that fosters teamwork.
• Excellent spoken and written communication.
• High energy and positive attitude toward working in a culturally diverse environment.
• Solution-oriented approach to customer support.
• Proactive approach and ownership of tasks from start to finish.

Work Locations

• Research Associate I: Bengaluru, India – Hybrid
• Coverage Analyst II: Bengaluru, India – Hybrid
• TEMP Research Consultant: Bengaluru, India – On-site

Application Details