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Fresher Opportunity at Advarra – Research Consultant Role Now Open

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Advarra – Research Consultant Role Now Open

Company: Advarra
Job Title: TEMP Research Consultant
Job Category: Research
Location: Bengaluru, India
Job Type: Full-Time | On-Site
Requisition Number: TEMPR003621


🔬 About Advarra

Advarra is a global leader in advancing clinical research through ethical review services, cutting-edge technology, and a deep understanding of industry needs. With a strong commitment to accelerating trials and improving human health, Advarra aligns all key stakeholders—patients, sponsors, CROs, and research sites—into a connected research ecosystem.


🧩 Company Culture

At Advarra, employees are the core of its mission-driven journey. The company fosters a culture that values patient-centricity, ethics, quality, and collaboration. Diversity is embraced, and every individual is empowered to thrive. Respect, empathy, and teamwork are key elements of daily work at Advarra, ensuring a positive and impactful environment.


💼 Key Responsibilities

  • Interpret clinical trial protocols to design and develop study calendars.
  • Review clinical trial agreements and sponsor budgets to create site-specific budgets.
  • Design case report forms (CRFs) based on protocol requirements.
  • Utilize Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) systems effectively.
  • Collaborate with the reporting manager to ensure deliverables meet quality standards and timelines.
  • Use internal systems to track and manage daily work assignments.
  • Actively participate in team meetings and contribute to protocol-related discussions.

📌 Location

This is an on-site position based in Bengaluru, India.


✅ Basic Qualifications

  • Understanding of clinical research methodology, regulations, and Good Clinical Practice (GCP).
  • Strong organizational and administrative skills.
  • Familiarity with MS Office and other business tools.
  • Ability to work independently and as part of a team.

⭐ Preferred Qualifications

  • 0–1 year internship experience in:
    • Clinical Trial Coordination
    • Clinical Data Management
    • Pharmacovigilance
    • Records Management
  • Excellent communication (spoken and written).
  • Proactive mindset with a strong sense of ownership.
  • High energy and a solutions-oriented attitude.
  • Ability to work in a culturally diverse environment.

🧠 Physical and Mental Requirements

  • Ability to sit or stand for extended periods at a workstation.
  • Capable of carrying, raising, and lowering objects up to 10 lbs.
  • Good focus, comprehension, and verbal communication skills.

🌟 Why Join Advarra?

At Advarra, you’re not just taking a job—you’re making a difference in the future of healthcare. Join a passionate team working toward a healthier, happier world by transforming the way clinical research is conducted.


Apply now and be part of a team that’s shaping the future of clinical research!

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