Research Associate I Job at Advarra in Bengaluru
An Advarra Research Associate opportunity is available in Bengaluru. This full-time, hybrid Research Associate I role is ideal for life science graduates with 0–1 year of experience in clinical research operations.
About Advarra
Advarra is a leading clinical research organization specializing in providing comprehensive research services to the pharmaceutical and biotechnology industries. With a focus on quality and innovation, Advarra operates globally, ensuring the successful execution of clinical trials while adhering to regulatory standards and best practices.
Job Details:
Position: Research Associate I
Location: Bengaluru, India
Requisition Number: RESEA004688
Employment Type: Full-time, Hybrid
Posted On: 08 October 2026
Advarra Research Associate Job Description
In this Advarra Research Associate role, the Research Associate I will be responsible for interpreting clinical trial protocols to design calendars, as well as interpreting clinical trial agreements and sponsor budgets to develop site budgets. The role also involves designing case report forms and working with Advarra’s Clinical Trial Management System (CTMS) and Electronic Data Capture (EDC) software. The candidate will complete calendars, budgets, financials, and case report forms to meet quality criteria, track assignments in case management software, and participate in team meetings regarding customer cases and protocols.
Key Responsibilities
- Interpret clinical trial protocols to design calendars.
- Interpret clinical trial agreements and sponsor budgets to develop site budgets.
- Design case report forms.
- Work in Advarra’s CTMS and EDC software.
- Complete calendars, budgets, financials, and CRFs to quality criteria.
- Track assignments in case management software.
- Join team meetings on customer cases and protocols.
Eligibility Criteria
- Knowledge of clinical research methodology, industry regulations, and Good Clinical Practice (GCP).
- Able to work independently and collaboratively within a team.
- Good organizational and administrative skills.
- Proficiency in MS Office.
Preferred Experience
- 6 months to 1 year as a Clinical Trial Coordinator at a site.
- Experience in Clinical Data Management, Pharmacovigilance, or Records Management.
How to Apply
Interested candidates can apply through Advarra’s official UKG/UltiPro careers board by following the link below:
CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
Conclusion
This Advarra Research Associate position presents an excellent opportunity for life science graduates to begin their careers in clinical research. Qualified candidates are encouraged to apply before the deadline to seize this chance to contribute to impactful clinical trials.
