Advarra Hiring – TEMP Research Consultant | Banglore
Advarra is hiring for the role of Temporary Research Consultant in Bangalore. This opportunity is suitable for candidates who are interested in clinical research, regulatory support, and research compliance activities. The role provides exposure to structured research processes and supports projects that focus on ethics, regulatory review, and research operations.
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🏢 About the Company
Advarra is an organization that supports clinical research through regulatory review, ethics oversight, and research compliance solutions. The company works closely with research institutions, sponsors, and clinical teams to ensure studies are conducted according to required guidelines. Professionals working at Advarra gain exposure to regulated research environments and quality‑driven workflows.
📊 Role 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
📋 Role & Responsibilities – TEMP Research Consultant at Advarra
- Supporting research documentation and review activities
- Assisting with compliance‑related research tasks
- Coordinating with internal teams on assigned projects
- Reviewing research‑related information for accuracy
- Maintaining organized records and tracking activitiesFollowing standard procedures and quality guidelines
🎓Qualification Required
- 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.
🧠 Skills Needed
- Knowledge of research documentation processes
- Organizational and coordination skills
- Analytical thinkingTime management abilities
- Ability to work in a compliance‑focused environment
⭐ Job Role Insight
- The Temporary Research Consultant role allows candidates to gain insight into how research projects are reviewed, supported, and managed within regulated environments. This experience helps professionals understand the importance of compliance, documentation accuracy, and coordination in clinical research, making it a valuable stepping stone for long‑term careers in research operations or regulatory support.
🎯 Ideal Candidates
- Fresh graduates interested in clinical research
- Candidates with research or documentation experience
- Professionals seeking short‑term or contract roles
- Individuals looking to enter regulated research environments
📈 Career Opportunities
Experience gained in this role can lead to future opportunities such as:
- Research Consultant
- Clinical Research Coordinator
- Regulatory or Compliance Support Roles
- Research Operations Associate
🔗 Application Process
Interested candidates should apply only through the official company career website using the link provided below.
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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Also read: Future of clinical research in India
❓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.
