Advarra Hiring TEMP Research Consultant | Bengaluru | Freshers Eligible
Are you seeking Advarra Careers Bengaluru or a Clinical Trial Operations Job for Freshers? Global ethical review and clinical research technology leader Advarra is hiring a TEMP Research Consultant for its Bengaluru office.
This clinical operations position is ideal for pharmacy and life science freshers looking to build a career in clinical study setup, calendar building, Case Report Form (CRF) design, and site budgeting. To build a standard resume indicating clinical trial operations coursework, read our guide on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | Advarra |
| Position | TEMP Research Consultant |
| Job Location | Bengaluru, Karnataka, India (On-site) |
| Department | Clinical Trial Operations / Consulting Services |
| Employment Type | Full-Time / Temporary Contract |
| Experience Required | 0 – 1 Years (Freshers Eligible) |
| Qualifications | B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc in Life Sciences or relevant fields |
| Salary (Indicative) | ₹3,00,000 – ₹6,00,000 per annum (Based on skills) |
💼 Key Responsibilities
- Study Calendar Design: Read and interpret clinical trial protocols to design and develop structured study calendars.
- Site Budget Creation: Review clinical trial agreements and sponsor budgets to generate site-level clinical budgets.
- CRF Development: Design and build Case Report Forms (CRFs) for study collection variables.
- System Administration: Utilize Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC) tools.
- Deliverables Tracking: Support reporting managers to deliver study calendars, budgets, financials, and CRFs within quality timelines.
- Operations Support: Track daily and weekly case details using internal case management systems.
- Team Collaboration: Participate in clinical team discussions to coordinate protocols and address customer requirements.
To learn how clinical operations support salaries compare to pharmacovigilance and drug safety tracking roles, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
- Education: Bachelor's or Master's degree in Pharmacy (B.Pharm, M.Pharm, Pharm.D), Life Sciences (B.Sc, M.Sc in Biotechnology, Microbiology, Biochemistry, etc.).
- Methodology Knowledge: Basic understanding of clinical trial phases, Good Clinical Practice (GCP) guidelines, and clinical databases.
- Software Literacy: Proficiency in Microsoft Office (specifically Word and Excel) and business database systems.
- Preferred Trainee Tracks: 0-1 year internship or trainee experience in Clinical Trial Coordination, Clinical Data Management (CDM), Pharmacovigilance (PV), or records management.
- Communication: Good written and verbal English communication skills for collaborating with global study managers.
For pharmacy graduates evaluating clinical database coordination pathways compared to conventional formulation tracks, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join Advarra?
- Opportunity to work with a leading global clinical research technology and institutional review board (IRB) provider.
- Gain hands-on skills in database technologies (CTMS, EDC, CRF design) and financial operations (study budgeting).
- Collaborative and mentorship-driven work environment.
- Build a solid career foundation in global clinical research and operations.
To test your clinical trial definitions, database setups, and GCP protocol knowledge, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Clinical Operations vs Healthcare IT
Research Consultants interpret trial protocols to configure study calendars and site budgets in database platforms, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for Advarra Candidates
- Highlight Protocol Review Skills: Detail any academic assignments or projects where you read clinical trial protocols, case studies, or scientific publications.
- Specify Software Skills: Explicitly mention database systems, spreadsheets, or case tracking systems you used during college or internships.
- Indicate Attention to Detail: Emphasize experience managing databases, reconciling numbers, or auditing documentation accuracy.
💬 Advarra TEMP Research Consultant Interview Questions
- Q1. What is a Case Report Form (CRF) and how does it relate to the study calendar?
Answer Guidance: A CRF is a clinical trial document designed to record all protocol-required data on each participant. The study calendar maps the schedule of events (patient visits, laboratory testing, dosing), indicating at which intervals specific CRFs must be completed. - Q2. How do you ensure accuracy when translating a protocol into a study calendar?
Answer Guidance: I review the Schedule of Events in the study protocol, identify all required patient procedures and visit windows, build the calendar sequence step-by-step, and perform a cross-referencing audit to ensure no visit or test is omitted. - Q3. What is the role of a CTMS (Clinical Trial Management System) in site operations?
Answer Guidance: A CTMS is a customized database system used to manage the administrative and financial aspects of clinical trials, including tracking investigator milestones, site budgets, enrollment logs, and documentation verification.
🚀 How to Apply?
Interested and eligible candidates can submit their applications directly via Advarra's recruiting portal. Click the button below to apply:
Apply Online – Advarra Recruiting Portal❓ Frequently Asked Questions
Q. What is the experience required for this Advarra research consultant position?
The role is open to freshers (0 to 1 year of experience). Relevant internships or training in clinical trials, CDM, or PV are preferred.
Q. What is the working model for this Bengaluru opportunity?
This is a full-time, on-site position based at Advarra's office in Bengaluru, Karnataka, India.
Q. What is the salary offered for this TEMP position?
The indicative salary range is ₹3.0 LPA to ₹6.0 LPA, based on qualifications and interview performance.
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