Clinical Trials Research Associate Fresher Vacancies Bangalore

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: RESEA003102

Job Location: Bengaluru, India

Job Description

About the Department & Responsibilities

As a Research Associate I at Advarra, your primary duties and responsibilities include:

Primary Duties and 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.

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:

• Fresher (0) to 01 year of work experience in areas such as clinical trial coordination, clinical data management, pharmacovigilance, or records management.

Apply online