Advarra Hiring Research Associate
A rare chance has emerged for aspiring research professionals: the Advarra Research Associate I role in Bengaluru is a full-time, hybrid opportunity to contribute to advancing clinical research and human health.
About Advarra
Advarra is a leading clinical research organization dedicated to improving human health through innovative research solutions. With a strong commitment to ethical practices and a focus on collaboration, Advarra connects patients, sites, sponsors, and CROs to streamline clinical trials. The organization prides itself on its rich history and expertise in the industry, making significant strides in clinical research.
Advarra Research Associate I Job Details
- Job Category: BOS RA
- The Advarra Research Associate I role involves developing clinical trial calendars, site budgets and case report forms.
- Requisition Number: RESEA004684
- Posted: 16 September 2026
- Location: Bengaluru – IND
Job Duties & Responsibilities
- Understand and interpret clinical trial study protocols to design and develop calendars. Understand and interpret clinical trial agreements and sponsor budgets to develop site budgets for the protocol.
- Design and develop case report forms for clinical trial study protocols.
- Develop a familiarity with Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software to utilize related functionalities in the design and development of calendars, budgets, financials and case report forms.
- Work closely with reporting manager to complete daily/weekly calendars, budgets, financials and/or case report forms design to meet with pre-determined quality criteria.
- Understand and utilize internal case management software and other reporting software to ensure that daily/weekly work assignments are appropriately tracked and completed.
- Actively participate in team meetings and contribute meaningfully to discussions related to specific customer cases and/or protocols.
Basic Qualifications
- Knowledge of clinical research methodology, industry regulations and Good Clinical Practice guidelines related to human research.
- Expected to work independently, as well as in a team environment.
- Good organizational and administrative abilities.
- Familiarity with MS Office and various business software.
Preferred Qualifications
- Preferred: 06 Months – 1 year work experience in job areas such as:
- Clinical trial coordinator at site.
- Clinical data management.
- Pharmacovigilance.
- Records management.
Physical and Mental Requirements
- Sit or stand for extended periods of time at stationary workstation.
- Regularly carry, raise, and lower objects of up to 5 kg.
- Learn and comprehend basic instructions.
- Focus and attention to tasks and responsibilities.
- Verbal communication; listening and understanding, responding, and speaking.
Advarra is an equal opportunity employer that is committed to providing a workplace that is free from discrimination and harassment of any kind based on race, color, religion, creed, sex (including pregnancy, childbirth, and related medical conditions, sexual orientation, and gender identity), national origin, age, disability or genetic information or any other status or characteristic protected under applicable laws in India.
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This Advarra Research Associate I opportunity presents a significant chance for qualified candidates to contribute to impactful clinical research. Interested individuals are encouraged to apply at the earliest to be part of a team dedicated to advancing human health through innovative solutions.
