Advarra Hiring Research Consultant (Clinical Research) | Freshers Eligible
🏢 About Advarra
Advarra is a global leader in clinical research support services, providing ethical review solutions, technology platforms, and research compliance services.
The company connects sponsors, CROs, sites, and patients to accelerate clinical trials and ensure ethical research practices.
📌 Job Overview
Position: Research Consultant (TEMP)
Location: Bangalore
Experience: 0–1 Year
Qualification: Life Sciences / Pharmacy Graduates
Industry: Clinical Research & Study Start-Up
🔬 Role Summary
This role supports clinical research operations including IRB submissions, safety reporting, and study start-up workflows.
If you are preparing for a career in clinical trials and data workflows, you can strengthen your knowledge using this Clinical SAS Quiz to understand clinical data structures.
Candidates interested in safety reporting processes may also test their knowledge through this Drug Safety Analyst Quiz covering safety reporting workflows.
🧾 Key Responsibilities
- Support Client Services using CTMS, IRB & CIRBI platforms
- Assist with translation management & safety reporting
- Support ongoing reviews & IRB submissions
- Document issues & manage customer responses
- Support Study Start-Up workflows
- Monitor and resolve customer escalations
- Track cases using internal case management systems
- Meet productivity & quality metrics
- Participate in team discussions & protocol reviews
🎓 Basic Qualifications
- Knowledge of clinical research methodology & GCP guidelines
- Strong organizational & administrative skills
- Ability to work independently and in teams
- MS Office & business software proficiency
⭐ Preferred Qualifications
- 0–1 year internship in clinical research or study start-up
- Experience in IRB submissions or regulatory processes
- Clinical data management exposure
- Strong written & verbal communication skills
- Problem-solving & customer support mindset
💼 Work Environment & Skills
- Ability to sit/stand for extended periods
- Attention to detail & focus
- Ability to handle multiple tasks
- Collaborative & ethical research environment
🌍 Why Join Advarra?
- Global exposure to clinical research operations
- Work on IRB & study start-up processes
- Strong foundation for CRO careers
- Collaborative & ethical work culture
- Opportunity to grow in regulatory & clinical operations
This role focuses on clinical research operations and study start-up workflows. Reviewing clinical research fundamentals and safety reporting concepts can improve your chances of success.
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