Advarra Hiring TEMP Research Consultant - Bengaluru
Are you seeking entry-level Advarra Clinical Trial Operations Jobs or Research Consultant Careers in Bangalore? Global leader in ethical review services and clinical trial technology Advarra has announced recruitment for a TEMP Research Consultant based at its Bengaluru facility. This is an excellent opportunity for freshers and early-career professionals (0-1 years of experience) to gain hands-on training.
This role allows graduates in pharmacy, life sciences, or biotechnology to develop study calendars, design Case Report Forms (CRFs), and coordinate study budgets using modern CTMS and EDC technologies. To prepare your application, check out our guide on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particulars | Details |
|---|---|
| Position | TEMP Research Consultant |
| Company | Advarra |
| Location | Bengaluru, Karnataka, India (On-site) |
| Employment Type | Full-Time (Contract) |
| Experience Required | 0 - 1 Years (Freshers Eligible) |
| Qualifications | B.Pharm, M.Pharm, Pharm.D, B.Sc & M.Sc in Life Sciences |
| Department | Clinical Trial Operations |
| Expected Salary | ₹3,00,000 – ₹5,00,000 per annum (Indicative) |
| Application Deadline | Apply Immediately (Not Mentioned) |
💼 Key Responsibilities
- Interpret clinical trial protocols to design and develop study calendars.
- Review clinical trial agreements and sponsor budgets to create site-level operational budgets.
- Design and develop Case Report Forms (CRFs) for clinical studies.
- Utilize Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC) tools.
- Work closely with reporting managers to deliver calendars, budgets, financials, and CRFs within quality timelines.
- Track daily and weekly deliverables using internal case management and reporting tools.
- Participate actively in team discussions related to protocols and customer cases.
Navigating CTMS platforms and understanding trial operations require a solid understanding of GCP principles. To test your clinical operational knowledge, try our interactive Clinical Trial Assistant (CTA) Quiz.
🎓 Qualifications & Experience Requirements
Candidates applying for this entry-level research consultant position should meet the following:
- Degrees: B.Pharm, M.Pharm, Pharm.D, B.Sc or M.Sc in Life Sciences or other relevant Life Sciences qualifications.
- Experience: 0 to 1 year of experience (freshers and interns preferred).
- Prior internship or trainee experience in Clinical Trial Coordination, Clinical Data Management, Pharmacovigilance, or Records Management is highly desirable.
For pharmacy graduates planning their career and comparing national vs global salary growth, check our guide on B.Pharm Career: India vs USA.
Required Core Skills
- Basic knowledge of clinical research methodology, GCP guidelines, and regulatory requirements.
- Ability to work independently and collaborate in global, culturally diverse team environments.
- Strong organizational, administrative, and problem-solving skills.
- High attention to detail and proactive work approach.
- Excellent written and verbal communication skills in English.
- Proficiency in MS Office and business software.
💰 Salary & Employee Benefits
- Expected Salary Package: ₹3.0 LPA – ₹5.0 LPA (Indicative, based on candidate's skills and internship exposure).
- Direct entry into a global clinical research organization and ethical review technology leader.
- Hands-on training and exposure to CTMS, EDC, study budgets, and CRF design.
- Strong learning and mentorship-driven work culture.
- Modern, inclusive, and patient-centric work environment.
To learn about typical roles and career progressions in clinical trial site operations, read our Clinical Research Coordinator (CRC) Guide.
🌟 Why Join Advarra?
- Advarra is a global leader in clinical research compliance, review services, and clinical trial technologies.
- Excellent launchpad for freshers to build a solid career foundation in clinical operations, data management, and regulatory affairs.
- Mentorship-focused work culture with opportunities to learn and collaborate with global clinical teams.
📑 Resume Tips for Advarra
- Highlight any GCP training certificates, clinical operations courses, or EDC/CTMS exposure.
- Emphasize your written and verbal English communication capabilities.
- Keep your resume clean, professional, and optimized for ATS systems.
🎯 Advarra Research Consultant Interview Questions
- What is a Case Report Form (CRF) and why is it important in clinical data collection?
- What is a Clinical Trial Management System (CTMS), and how does it assist trial operations?
- How do you construct an operational site budget from a sponsor clinical trial agreement?
- What are the core principles of Good Clinical Practice (GCP)?
- Describe your experience working with MS Office tools like Word and Excel.
📌 How to Apply?
Interested and eligible candidates can submit their applications online directly through Advarra's official job recruitment portal using the link below. Since no specific application deadline is mentioned, candidates are advised to apply immediately. For step-by-step guidance on setting up your application profile, read our guide on how to apply for healthcare and pharma jobs online.
🚀 Apply Now
Apply Online❓ Frequently Asked Questions
Q. What is the application deadline?
No deadline is mentioned in the official post. Candidates are advised to apply immediately.
Q. Who is eligible to apply?
B.Pharm, M.Pharm, Pharm.D, and B.Sc/M.Sc Life Sciences graduates.
Q. What is the required experience?
No prior experience is required; this is an entry-level position open to freshers and interns (0-1 years of experience).
.png)
