At Advarra, we are passionate about making a difference in the world of clinical research and advancing human health. With a rich history rooted in ethical review services combined with innovative technology solutions and deep industry expertise, we are at the forefront of industry change. A market leader and pioneer, Advarra breaks the silos that impede clinical research, aligning patients, sites, sponsors, and CROs in a connected ecosystem to accelerate trials.

Job Overview

Job Summary: Advarra is hiring a Clinical Research Associate to support the development of clinical research services in Bengaluru.

Company Profile: Advarra is committed to advancing human health by providing ethical review services and innovative technology solutions for clinical research.

Detailed Job Description

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.

Location

This role is open to candidates working remotely or hybrid in Bengaluru, India.

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: 0-1 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 a stationary workstation.
• Regularly carry, raise, and lower objects of up to 10 lbs.
• Learn and comprehend basic instructions.
• Focus and attention to tasks and responsibilities.
• Verbal communication; listening and understanding, responding, and speaking.

How to Apply

Interested candidates are invited to apply by submitting their resume and cover letter.

Apply Online

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