Research Associates Job Vacancies in Bangalore

Research Associates Job Vacancies in Bangalore

Are you a skilled Research Associate seeking new opportunities in the dynamic field of clinical research? Advarra’s India Operations team is expanding, and we are conducting a walk-in recruitment drive for experienced professionals like you! Join our global organization with a commitment to ethics, an inclusive work culture, and a focus on employee well-being.

About Advarra

Advarra, a global leader in clinical research, is at the forefront of innovation, working with leading Pharma companies, CROs, and research sites. Our Bengaluru-based team has grown significantly, comprising over 200 clinical research professionals dedicated to excellence.

Company (Advarra) Vacancies List

Position Title: Research Associate I/II/III

Company Name: Advarra India Private Limited

Salary: Competitive

Company Address: No. 2 (Old No. 4), 6th floor, Prestige Emerald, Madras Bank Road, Lavelle Road, Bengaluru – 560001

Job Description

Role: Research Associate

Industry Type: Clinical Research

Department: Clinical Operations

Employment Type: Full-time

Role Category: Clinical Research

Educational Background Required: Bachelor’s Degree in Life Sciences

Key Skills: Clinical Trial Coordination, Data Management, Pharmacovigilance, Records Management

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

• 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: 0-1 year work experience in job areas such as: o Clinical trial coordinator at site
• Clinical data management
• Pharmacovigilance
• Records management

Preferred Qualifications

• Preferred: 0-1 year work experience in job areas such as:
• Clinical trial coordinator at site
• Clinical data management
• Pharmacovigilance
• Records management

Apply online

Tagged as: Clinical Operations, Clinical Research, Clinical Trial Management