Advarra Hiring – TEMP Research Consultant | Banglore

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Advarra, a global provider of research compliance and clinical research solutions, is hiring for the role of TEMP Research Consultant at its Bengaluru location. This opportunity is suitable for B.Pharm, M.Pharm, B.Sc, and M.Sc graduates with 0–1 year of experience who are looking to start their career in clinical research support and research operations.

The role focuses on supporting research review processes, study documentation, compliance activities, and coordination with internal research teams in a regulated environment. Candidates will gain hands‑on exposure to clinical research workflows, regulatory compliance, and operational support activities.

This is a strong entry‑level, temporary opportunity for early‑career professionals seeking experience with a globally recognized organization in the clinical research and healthcare compliance space.

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Job Overview

  • Position: TEMP Research Consultant
  • Department: Clinical research
  • Location: Bengaluru
  • Experience: 0 to 1 years
  • Qualification: M.Pharm, M.Sc, B.pharm, B.sc
  • Job Type: Full-Time
  • Last Date of application: Not provided

Key Responsibilities – TEMP Research Consultant at Advarra

  • Review, understand, and interpret clinical trial study protocols to design and develop study calendars.
  • Interpret clinical trial agreements and sponsor budgets to develop accurate site budgets aligned with protocol requirements.
  • Design and develop Case Report Forms (CRFs) based on clinical trial study protocols.
  • Build familiarity with Advarra Clinical Trial Management System (CTMS) and Electronic Data Capture (EDC) systems.
  • Use system functionalities to support development of calendars, budgets, financials, and CRFs.
  • Work closely with the reporting manager to complete daily and weekly assignments related to calendars, budgets, financials, and CRF design in line with pre‑defined quality standards.
  • Use internal case management and reporting tools to track work assignments and ensure timely completion of tasks.
  • Actively participate in team meetings and contribute to discussions related to customer cases and study protocols..

Required Skills & Qualifications

  • 0–1 year of internship experience in one or more of the following areas is preferred:
    • Clinical Trial Coordinator (site‑level)
    • Clinical Data Management
    • Pharmacovigilance
    • Records or Document Management
  • Highly personable and collaborative nature that supports teamwork and positive working relationships.
  • Ability to work effectively within cross‑functional and culturally diverse teams.
  • Excellent written and verbal communication skills, with the ability to clearly explain information and support stakeholder interactions.
  • High energy and positive attitude, with enthusiasm for learning and contributing in a dynamic environment.
  • Strong commitment to delivering outstanding customer support with a solution‑oriented mindset.
  • Proactive approach with the ability to take ownership of tasks from start to finish.

Why join Advarra?

  • The TEMP Research Consultant role is ideal for freshers and early‑career professionals, offering hands‑on exposure to clinical research support, study setup, and operational workflows.
  • Gain practical experience with Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC) platforms, and internal case‑management tools used across global studies.
  • Advarra provides a structured environment to develop skills in protocol interpretation, calendar and budget development, CRF design, and clinical research documentation.
  • Work in a highly collaborative, diverse, and supportive team environment, where teamwork, communication, and shared learning are encouraged.
  • Contribute directly to outstanding customer support and high‑quality research operations, helping ensure compliant and efficient clinical trials.

How to Apply

Interested candidates should apply only through the official company career website using the link provided below.

Apply Here

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.

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FAQ – TEMP Research Consultant at Advarra

1. Who can apply for the TEMP Research Consultant role at Advarra?

Candidates with B.Pharm, M.Pharm, B.Sc, or M.Sc degrees and 0–1 year of experience (including internships) are eligible to apply.

2. Is this role suitable for freshers?

Yes. This is an entry‑level, temporary position designed for freshers and early‑career professionals seeking experience in clinical research operations.

3. What kind of work will I perform in this role?

You will support clinical trial operations by developing study calendars, site budgets, and CRFs, and by assisting with CTMS/EDC system activities and case management tasks.

4. Is prior clinical research experience required?

Prior experience is not mandatory. However, internships or exposure in clinical trial coordination, data management, pharmacovigilance, or records management are preferred.

5. Will I work with CTMS and EDC systems?

Yes. You will gain hands‑on exposure to Advarra’s CTMS and EDC systems, helping design and manage calendars, budgets, financials, and CRFs.

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