Advarra is Hiring TEMP Research Consultant in Bengaluru
A rare chance has emerged for aspiring clinical research professionals as Advarra opens applications for the Advarra Research Consultant position in Bengaluru, India. This full-time, on-site role is ideal for candidates with 0–1 year of relevant experience, offering an opportunity to engage in various clinical research operations.
About Advarra
Advarra is a leading clinical research organization that specializes in providing comprehensive services to the pharmaceutical and biotechnology industries. With a commitment to advancing clinical trials, Advarra operates globally, focusing on delivering high-quality research solutions that ensure patient safety and regulatory compliance. The organization is known for its innovative approach and dedication to enhancing the efficiency of clinical studies.
Job Details:
Position: TEMP Research Consultant
Type: Temporary
Location: Bengaluru, India
Requisition Number: TEMPR004761
Posted On: 08 October 2026
Employment Type: Full-time, On-site
Advarra Research Consultant Job Description
The Advarra Research Consultant will be responsible for learning Advarra’s CTMS, IRB, and CIRBI platforms, supporting Client Services in various tasks including translation management, safety reporting, ongoing reviews, site termination, and IRB submissions. This role also involves documenting issues and customer responses, supporting high-turnaround study start-up, monitoring customer escalations, and meeting daily and weekly quality and productivity metrics.
Key Responsibilities
- Learn Advarra’s CTMS, IRB, and CIRBI platforms.
- Support Client Services in translation management and safety reporting.
- Assist with ongoing reviews, site termination, and IRB submissions.
- Document issues and customer responses.
- Support high-turnaround study start-up.
- Monitor and help resolve customer escalations.
- Meet daily and weekly quality and productivity metrics.
Advarra Research Consultant Eligibility Criteria
- Knowledge of clinical research methodology and regulations.
- Understanding of study start-up and Good Clinical Practice (GCP).
- Good organizational and administrative skills.
- Proficiency in MS Office.
Required Skills
- 0–1 year of internship experience as a site Clinical Trial Coordinator (CTC), in study start-up, regulatory affairs, or clinical data management.
- Experience with IRB/ethics committee submissions.
- Records management experience is preferred.
How to Apply
Interested candidates can apply through Advarra’s official UKG/UltiPro careers board by following this link: CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE.
Why Join Advarra
Joining Advarra offers a unique opportunity to be part of a dynamic team that is at the forefront of clinical research. The organization values innovation, collaboration, and professional growth, providing employees with the tools and support needed to excel in their careers. Advarra’s commitment to quality and patient safety makes it an ideal place for aspiring professionals to develop their skills and contribute to meaningful research.
Conclusion
This Advarra Research Consultant opportunity is an excellent option for candidates looking to start their careers in clinical research with Advarra. Qualified individuals are encouraged to apply before the deadline to secure their chance to be part of a leading organization in the industry.
