Advarra is hiring a Research Associate II for a full-time, hybrid position in Bengaluru, India. This opportunity is ideal for professionals with experience in clinical research, clinical data management (CDM), pharmacovigilance (PV), clinical trial coordination, or records management.
The Research Associate II will support clinical trial operations by interpreting study protocols, developing study calendars and site budgets, designing Case Report Forms (CRFs), and working with Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC) platforms.
With the growing demand for skilled clinical research professionals in India, this Advarra Research Associate II job in Bengaluru offers an opportunity to build expertise across clinical trial operations, protocol interpretation, clinical data, budgets, and research technology.
Job Highlights
- Company: Advarra
- Job Title: Research Associate II
- Job Category: BOS RA
- Requisition Number: RESEA004680
- Job Type: Full-time
- Work Mode: Hybrid
- Location: Bengaluru, India
- Experience Required: 1+ years
- Posted Date: September 9, 2026
- Application Deadline: October 9, 2026
About Advarra
Advarra is a clinical research technology and services organization focused on advancing human health and improving the clinical research ecosystem. The company supports the connection between patients, clinical research sites, sponsors, and Contract Research Organizations (CROs).
Advarra combines expertise in ethical review, clinical research operations, and technology solutions to help improve and accelerate clinical trials. Its work focuses on creating a more connected clinical research environment while maintaining strong standards for quality, ethics, and patient-centric research.
The company’s culture emphasizes four core principles:
- Patient-Centric
- Ethical
- Quality Focused
- Collaborative
Research Associate II Job Description
As a Research Associate II at Advarra, you will contribute to the design and operational setup of clinical trials. The role involves understanding clinical study protocols and translating study requirements into calendars, budgets, financial workflows, and Case Report Forms.
You will also gain exposure to important clinical research technologies, including Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC) systems.
This role requires strong attention to detail, organizational abilities, knowledge of clinical research methodology, and the ability to work independently and collaboratively.
Key Responsibilities
The selected candidate will be responsible for:
1. Clinical Protocol Interpretation
- Understand and interpret clinical trial study protocols.
- Analyze protocol requirements for clinical trial implementation.
- Support the development of study-related calendars and research documentation.
2. Clinical Trial Calendar Development
- Design and develop calendars based on clinical trial protocols.
- Ensure study calendars meet predefined quality requirements.
- Complete assigned calendar-related activities within required timelines.
3. Site Budget Development
- Interpret clinical trial agreements.
- Review sponsor budgets.
- Support the development of site budgets based on clinical trial protocols.
- Assist with financial and budget-related clinical trial activities.
4. Case Report Form (CRF) Development
- Design and develop Case Report Forms (CRFs) for clinical trial protocols.
- Support accurate translation of protocol requirements into CRF structures.
- Work with relevant systems and processes supporting clinical data collection.
5. CTMS and EDC Systems
- Develop familiarity with Advarra’s Clinical Trial Management Software (CTMS).
- Learn and utilize Electronic Data Capture (EDC) software.
- Use relevant software functionalities for calendars, budgets, financials, and CRF development.
6. Quality and Productivity
- Work closely with the reporting manager.
- Complete daily and weekly assignments within established timelines.
- Ensure work meets predetermined quality criteria.
- Maintain accuracy and attention to detail across assigned activities.
7. Case Management and Reporting
- Utilize internal case management systems.
- Track daily and weekly work assignments.
- Ensure assigned activities are appropriately documented and completed.
- Use reporting software as required.
8. Team Collaboration
- Participate actively in team meetings.
- Contribute to discussions involving customer cases and clinical trial protocols.
- Collaborate effectively with colleagues and managers.
Qualifications for Advarra Research Associate II
Candidates applying for this Research Associate II job in Bengaluru should meet the following requirements.
Basic Qualifications
- Minimum 1+ years of relevant experience.
- Knowledge of clinical research methodology.
- Understanding of industry regulations related to human research.
- Knowledge of Good Clinical Practice (GCP) guidelines.
- Ability to work independently.
- Ability to work effectively in a team environment.
- Strong organizational and administrative skills.
- Familiarity with Microsoft Office.
- Familiarity with business and workplace software.
- Strong attention to detail and task management skills.
Preferred Experience
Candidates with experience in the following areas may have an advantage:
- Clinical Trial Coordination
- Clinical Data Management (CDM)
- Pharmacovigilance (PV)
- Records Management
Experience at a clinical research site, hospital research department, CRO, pharmaceutical company, or clinical research organization may be particularly relevant.
Educational Qualification
The job description does not specify a mandatory degree. However, candidates with relevant education or professional backgrounds in the following areas may be suitable:
B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Life Sciences, Biotechnology, Clinical Research, Nursing, Medicine, or other relevant healthcare and life sciences disciplines.
Candidates should carefully review the official job posting before applying.
Experience Required
Minimum Experience: 1+ years of relevant experience
Relevant experience may include work in:
- Clinical Research
- Clinical Trial Coordination
- Clinical Data Management
- Pharmacovigilance
- Site Management
- Clinical Operations
- Records Management
- Clinical Trial Documentation
Skills Required
The ideal candidate should possess knowledge or skills in:
- Clinical Research Methodology
- Clinical Trial Protocols
- Good Clinical Practice (GCP)
- Clinical Trial Regulations
- Case Report Forms (CRFs)
- Clinical Trial Management Systems (CTMS)
- Electronic Data Capture (EDC)
- Clinical Trial Documentation
- Site Budgets
- Study Calendars
- Microsoft Office
- Organizational Skills
- Attention to Detail
- Communication Skills
- Team Collaboration
Salary for Research Associate II at Advarra
The official job posting does not disclose the salary for this position.
Based on the job title, Bengaluru location, required experience, and responsibilities, the estimated salary range for a Research Associate II in clinical research may be approximately โน4.5 lakh to โน8 lakh per annum.
Actual compensation may vary depending on:
- Candidate experience
- Educational qualifications
- Clinical research expertise
- Technical skills
- Previous employer
- Interview performance
- Advarra’s compensation structure
Note: This is an estimated salary range and has not been officially disclosed by Advarra.
Why Consider This Clinical Research Job?
This opportunity can be particularly valuable for professionals looking to gain or expand experience in multiple areas of clinical trial operations.
The role provides exposure to:
- Clinical trial protocols
- Study calendars
- Site budgets
- Clinical trial financial processes
- Case Report Form development
- CTMS platforms
- EDC systems
- Clinical research regulations
- Good Clinical Practice
For professionals from Clinical Data Management, Pharmacovigilance, Clinical Trial Coordination, or Clinical Research, the position may offer opportunities to develop broader clinical trial operations experience.
Work Location and Mode
๐ Location: Bengaluru, Karnataka, India
๐ผ Work Mode: Hybrid
๐ Employment Type: Full-time
Candidates applying for the Advarra Research Associate II position should be prepared to work in accordance with the company’s hybrid work requirements.
How to Apply
