💼 Research Consultant – Clinical Research | Advarra
🏢 Company: Advarra📍 Location: Bangalore, India
🎓 Eligibility: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Life Sciences
🧪 Experience: 0–1 Year (Freshers Welcome)
💰 Salary: Competitive (Industry Standard)
📝 Job Type: Full-Time | Clinical Research | On-site
🔎 Verified: ✅ Verified Job via Medical Jobs India – hitechplus.in
🏢 About Advarra
Advarra is a global leader in clinical research, dedicated to advancing human health through ethical review services, innovative technology, and deep industry expertise. The company plays a pivotal role in accelerating clinical trials by connecting patients, sites, sponsors, and CROs in a unified ecosystem.
🌟 Company Culture
Advarra fosters an inclusive and collaborative workplace where employees are valued and empowered. Their core values—Patient-Centric, Ethical, Quality-Focused, and Collaborative—drive their mission to improve clinical research outcomes. The company is committed to diversity, equity, and inclusion, ensuring a respectful and supportive environment for all employees.
📌 Key Responsibilities
- ✔ Gain familiarity with Advarra’s CTMS, IRB, and CIRBI systems to support Client Services teams.
- ✔ Assist in Translation Management, Safety Reporting, and Ongoing Reviews (Site Termination & IRB Submissions).
- ✔ Document issues, manage customer responses, and ensure efficient Study Start-Up processes.
- ✔ Monitor and resolve customer escalations promptly.
- ✔ Use internal case management software to track and complete assigned tasks.
- ✔ Participate in team meetings, contributing insights on customer cases and protocols.
✅ Eligibility & Skills
- ✅ Knowledge of clinical research methodology, GCP guidelines, and study start-up activities.
- ✅ Ability to work independently and collaboratively in a team.
- ✅ Strong organizational and administrative skills.
- ✅ Proficiency in MS Office and business software.
🎯 Preferred Qualifications
- 📌 0–1 year internship experience in clinical trial coordination, study start-up, regulatory affairs, IRB submissions, or data management.
- 📌 Excellent communication skills (written & verbal).
- 📌 Proactive attitude and ability to thrive in a diverse environment.
- 📌 Strong problem-solving skills and commitment to customer support.
💪 Physical & Mental Requirements
- 🪑 Ability to sit/stand for extended periods.
- 📦 Lift objects up to 10 lbs.
- 🧠 Strong focus, attention to detail, and verbal communication skills.
📌 Note Before You Apply:
Highlight your knowledge of GCP, clinical trial processes, and any relevant internship/project experience in your application.
👇 Application Link Will Be Visible in 15 Seconds 👇
🟢 Verified Job via Medical Jobs India – hitechplus.in
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