Advarra Clinical Research Job for Life Sciences Graduates | Research Associate II

Research Associate II Role at Advarra, Bengaluru – Clinical Research Job for Life Sciences Graduates with 1+ Year Experience

Join Advarra’s Research division as a Research Associate II in Bengaluru. Ideal for graduates in life sciences or pharmacy with 1+ year experience in clinical research, data management, or pharmacovigilance.

Research Associate II – Clinical Research Job in Bengaluru

Apply now for Research Associate II role at Advarra in Bengaluru. Life Sciences/Pharmacy graduates with 1+ yr experience eligible. Clinical research job.

Advarra, a leader in clinical research solutions, is seeking a Research Associate II for its Bengaluru office. This full-time, on-site opportunity is ideal for professionals with 1+ years of experience in clinical trials, pharmacovigilance, or data management.

This role offers a dynamic work environment focused on ethical, patient-centric research with cutting-edge technologies like CTMS and EDC.

About Advarra

Advarra is a global leader in advancing clinical research. From ethical reviews to technology-powered solutions, Advarra aligns sponsors, CROs, and sites to accelerate trial execution. The company prides itself on a collaborative, inclusive culture and emphasizes quality, ethics, and innovation.

Employees at Advarra are empowered to make a meaningful impact by enhancing the clinical research ecosystem.

Key Responsibilities

Calendar, Budget & Form Development

• Interpret clinical trial protocols and agreements
• Design clinical trial calendars and site budgets
• Develop case report forms aligned with protocol requirements

Software Tools & Collaboration

• Utilize CTMS and EDC tools
• Track assignments via internal case management systems
• Collaborate with teams on client-specific needs

Meetings & Documentation

• Actively participate in team discussions
• Ensure quality standards and deadlines are met

Required Qualifications

• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or Allied Health Sciences
• Minimum 1+ year of relevant experience
• Knowledge of clinical trial regulations, GCP, ICH guidelines
• Proficiency in MS Office and related business software
• Strong organizational, communication, and documentation skills

Preferred Experience

• Former Clinical Trial Coordinator, Clinical Data Manager, or Pharmacovigilance Specialist
• Familiarity with record management systems

Location & Work Mode

• Location: Bengaluru, India
• Type: Full-time, On-site (Hybrid option may be considered)

Application Process

Interested candidates can apply directly through the official Advarra career portal: Apply Here

Ensure to include your updated resume with relevant experience.

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