Advarra is hiring a TEMP Research Consultant for its Bengaluru (on-site) location. This is an excellent entry-level clinical research job for freshers and early-career professionals seeking hands-on exposure to clinical trial operations, CTMS, EDC, study calendars, site budgets, and case report form (CRF) design.
As a global leader in ethical review services and clinical research technology, Advarra plays a critical role in accelerating clinical trials while ensuring patient safety, regulatory compliance, and data quality. This opportunity is ideal for candidates aiming to build a long-term career in clinical research, clinical data management, or pharmacovigilance.
Key Responsibilities – TEMP Research Consultant
- Interpret clinical trial protocols to design and develop study calendars
- Review clinical trial agreements and sponsor budgets to create site-level 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
Qualifications & Skills
Basic Qualifications
- Knowledge of clinical research methodology, GCP, and regulatory requirements
- Ability to work independently and in team-based environments
- Strong organizational and administrative skills
- Proficiency in MS Office and business software
Preferred Qualifications
- 0–1 year internship or trainee experience in:
- Clinical Trial Coordination
- Clinical Data Management
- Pharmacovigilance
- Records Management
- Strong written and verbal communication skills
- High attention to detail and proactive work approach
- Customer-focused mindset with problem-solving abilities
- Comfortable working in a global, culturally diverse environment
Benefits of Working at Advarra
- Entry into a global clinical research organization
- Hands-on exposure to CTMS, EDC, study budgets, and CRF design
- Strong learning and mentorship-driven culture
- Inclusive, ethical, and patient-centric work environment
- Excellent career foundation for roles in clinical operations, data management, and regulatory affairs
Job Location
📍 Bengaluru, Karnataka (On-site)
Salary (Indicative)
💰 ₹3,00,000 – ₹6,00,000 per annum (INR, based on skills and experience)
How to Apply
