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Advarra Hiring: Clinical Trials Research Associate I – Golden Opportunity for Freshers
About the Advarra
Welcome to Advarra, a pioneer in advancing human research. At Advarra, we’re committed to driving excellence in clinical trials, ensuring the highest standards in research practices. Join us in our mission to contribute to groundbreaking research and make a difference in the world of healthcare.
Advarra Vacancies List
Position Title: Research Associate I
Company Name: Advarra
Job Category: Research
Requisition Number: RESEA002539
Job Location: Bengaluru, India
Job Description
About the Department & Responsibilities
As a Research Associate I at Advarra, your primary duties and responsibilities include:
- Clinical Trial Protocol Understanding:
- Interpret clinical trial study protocols to design and develop calendars.
- Trial Agreements and Budgets:
- Understand and interpret clinical trial agreements and sponsor budgets to develop site budgets for the protocol.
- Case Report Form Development:
- Design and develop case report forms for clinical trial study protocols.
- Clinical Trial Management Software (CTMS) and EDC:
- Develop familiarity with Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software for designing calendars, budgets, financials, and case report forms.
- Collaboration and Meetings:
- Actively participate in team meetings, contributing meaningfully to discussions related to specific customer cases and/or protocols.
Position Requirements
To excel in this role, you should possess:
- Knowledge of clinical research methodology, industry regulations, and Good Clinical Practice guidelines related to human research.
- Ability to work independently and collaboratively in a team environment.
- Good organizational and administrative abilities.
- Familiarity with MS Office and various business software.
Preferred:
- 0-1 year of work experience in areas such as clinical trial coordination, clinical data management, pharmacovigilance, or records management.
Apply online
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