Advarra is driven by a mission to accelerate clinical research and improve lives worldwide. As a pioneer in ethical review and clinical trial management, the company integrates patients, sites, sponsors, and CROs into a unified ecosystem. Guided by values of Patient-Centricity, Ethics, Quality Focus, and Collaboration, Advarra is committed to fostering inclusivity, empathy, and innovation in all its endeavors.
Key Responsibilities
As a Research Associate I, your primary duties will include:
- Interpreting clinical trial study protocols to design and develop calendars.
- Analyzing clinical trial agreements and sponsor budgets to create site budgets.
- Designing case report forms for study protocols.
- Utilizing Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) tools for calendar, budget, and financial design.
- Managing tasks with internal case management and reporting software to ensure deadlines are met.
- Collaborating in team meetings and contributing to case and protocol discussions.
Location
This role offers flexibility for remote or hybrid working arrangements based in Bengaluru, India.
Basic Qualifications
- Knowledge Base: Familiarity with clinical research methodology, industry regulations, and Good Clinical Practice (GCP) guidelines.
- Technical Skills: Proficiency in MS Office and related business software.
- Soft Skills: Strong organizational, administrative, and communication abilities.
- Team Dynamics: Ability to work independently and collaboratively.
Preferred Experience
While prior experience is not mandatory, candidates with 0-1 year of experience in areas such as:
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- Clinical trial coordination
- Clinical data management
- Pharmacovigilance
- Records management
are preferred.
