Advarra, a global leader in clinical research technology and ethics review solutions, is inviting applications for the position of TEMP Research Consultant in Bengaluru, India. This opportunity is ideal for fresh graduates and candidates with up to one year of internship or industry experience in Clinical Research, Clinical Data Management, Regulatory Affairs, IRB submissions, or Study Start-Up.
If you’re looking to begin your career in the clinical research industry, this Advarra hiring drive offers hands-on exposure to Clinical Trial Management Systems (CTMS), IRB processes, safety reporting, study start-up activities, and regulatory operations while working with global clinical research teams.
Job Details
- Position: TEMP Research Consultant
- Company: Advarra
- Location: Bengaluru, Karnataka, India
- Job Type: Full-Time
- Work Mode: Work From Office
- Department: Research
- Experience: Freshers / 0–1 Year Preferred
Key Responsibilities
- Support Clinical Trial Management Software (CTMS) and IRB platforms.
- Assist with translation management and safety reporting activities.
- Handle ongoing site reviews and site termination documentation.
- Support IRB and ethics committee submissions.
- Monitor customer queries and resolve escalations efficiently.
- Track daily work using internal case management systems.
- Maintain quality and productivity metrics.
- Collaborate with cross-functional teams on study start-up activities.
- Participate in team discussions and protocol reviews.
- Ensure compliance with GCP and clinical research regulations.
Eligibility Criteria
Candidates should possess knowledge of:
- Clinical Research methodology
- Good Clinical Practice (GCP)
- Clinical Trial processes
- Study Start-Up activities
- Industry regulations
- MS Office applications
- Administrative and organizational skills
Preferred Qualifications
Candidates having internship or practical exposure in any of the following areas are preferred:
- Clinical Trial Coordination
- Study Start-Up
- Regulatory Affairs
- IRB & Ethics Committee Submissions
- Clinical Data Management
- Records Management
Required Skills
- Excellent written and verbal communication
- Strong organizational skills
- Team collaboration
- Customer-focused mindset
- Positive attitude
- Ability to work independently
- Problem-solving skills
- Time management
- Attention to detail
Salary
Expected Salary: ₹4.8 – ₹7.2 LPA (Estimated based on similar Clinical Research entry-level roles in India.)
Why Join Advarra?
- Work with a global clinical research organization.
- Exposure to CTMS, IRB, and regulatory processes.
- Learn international clinical trial workflows.
- Opportunity to collaborate with global sponsors and CROs.
- Career growth in Clinical Research and Regulatory Operations.
- Inclusive and collaborative work culture.
- Excellent learning environment for fresh graduates.
How to Apply
