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Alimentiv is actively hiring for the role of IRT Coordinator (Interactive Response Technology) in India (Remote). This opportunity is ideal for candidates with 1–3 years of experience in clinical research, data management, or IRT systems who are looking to grow in global clinical trial operations.
In this role, you will support IRT system management, clinical trial randomization workflows, drug supply logistics, and eTMF documentation, ensuring compliance with ICH-GCP, GxP, and regulatory standards. If you want to build expertise in clinical data systems, UAT testing, and trial coordination, this is a high-growth role in the CRO domain.
Key Responsibilities – IRT Coordinator Role
Clinical Trial & IRT Project Support
- Assist in IRT documentation across trial lifecycle (start-up to maintenance)
- Draft IRT User Guides, UAT scripts, and test documentation
- Support User Acceptance Testing (UAT) and database validation
- Manage drug inventory tracking and ordering processes
- Generate and review clinical trial reports and data transfers
- Maintain electronic Trial Master File (eTMF) documentation
- Perform administrative tasks like report distribution and internal communications
- Coordinate client meetings and cross-functional discussions
- Provide technical/user support and issue escalation for IRT systems
Operational & Departmental Support
- Contribute to process improvements in IRT and Clinical Data Management (CDM)
- Participate in cross-functional teams (Clinical Ops, Biostatistics, Supply Chain)
- Promote IRT best practices and compliance standards
- Support training and knowledge-sharing initiatives
Required Qualifications
- Qualification: Diploma / Degree in Life Sciences, Pharmacy, or related field
- Experience: 1–3 years in clinical research, IRT, CDM, or trial coordination
- Strong understanding of:
- Clinical trial processes & protocols
- IRT systems (randomization, drug supply, data capture)
- ICH-GCP, GxP, and regulatory compliance
- Experience with:
- UAT testing, URS documentation, validation processes
- eTMF systems and clinical documentation
- Skills:
- Excellent communication & coordination skills
- Strong project tracking & timeline management
- Ability to collaborate across global teams & time zones
Preferred Skills (High-Impact for Selection)
- Knowledge of drug supply chain & IP labeling workflows
- Familiarity with randomization procedures in clinical trials
- Experience with IRT tools and reporting systems
- Exposure to clinical data transfers and system integrations
Salary & Benefits
- Estimated Salary: ₹4,50,000 – ₹8,00,000 per annum (based on experience)
- Work Mode: Remote (India)
- Opportunity to work with global clinical trials and CRO projects
- Exposure to IRT systems, eTMF, and advanced clinical technologies
- Career growth in Clinical Data Management & Clinical Operations
Why Join Alimentiv?
- Work on global clinical trials with cutting-edge IRT systems
- Gain expertise in randomization, drug supply, and clinical data workflows
- Strong exposure to cross-functional collaboration in CRO environment
- Build a future-proof career in clinical research technology
How to Apply
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