IRT Coordinator Remote Job at Alimentiv. Remote clinical research role with eTMF, IRT systems, and drug supply experience required.
Are you looking to build a career in clinical research technology and trial operations? Alimentiv is offering an exciting remote opportunity for an IRT Coordinator in India. This role is ideal for candidates with experience in clinical trials, data management, or IRT systems who want to gain global exposure and work on advanced clinical research platforms.
Company Overview
Alimentiv is a global contract research organization (CRO) specializing in clinical trials, imaging, and precision medicine. The company partners with pharmaceutical and biotechnology firms to support drug development through innovative technologies and data-driven solutions. Known for its expertise in gastrointestinal and inflammatory diseases, Alimentiv provides high-quality clinical research services worldwide.
Job Overview
| Job Title | IRT Coordinator (Clinical Research & TMF) |
|---|---|
| Company | Alimentiv |
| Location | Remote (India) |
| Employment Type | Full-Time |
| Department | Clinical Research / IRT / Data Management |
| Experience | 1–3 Years |
| Qualification | Life Sciences / Pharmacy |
| Salary | ₹4.5 LPA – ₹8 LPA (Estimated) |
| Application Mode | Online Application |
Job Location & Employment Type
- Work Location: Remote (Work from Home – India)
- Job Type: Full-time
- Work Mode: Remote with global team collaboration
Open Positions / Department Details
This role is part of the Interactive Response Technology (IRT) and Clinical Data Management team. The position focuses on managing clinical trial systems, randomization workflows, drug supply logistics, and maintaining regulatory-compliant documentation.
Key Roles & Responsibilities
As an IRT Coordinator, you will support clinical trial operations through system management, documentation, and coordination activities.
Clinical Trial & IRT System Support
- Assisting in IRT system documentation throughout the clinical trial lifecycle
- Preparing User Guides, UAT scripts, and validation documents
- Supporting User Acceptance Testing (UAT) and system validation processes
- Managing randomization workflows and trial data processes
- Generating and reviewing clinical trial reports and system outputs
Drug Supply & Data Management
- Tracking and managing investigational product (IP) inventory
- Supporting drug ordering and supply chain processes
- Handling clinical data transfers and ensuring data accuracy
- Maintaining compliance with study protocols and regulatory requirements
Documentation & eTMF Management
- Maintaining electronic Trial Master File (eTMF) documentation
- Ensuring proper filing and organization of clinical trial documents
- Supporting audit readiness and documentation completeness
Coordination & Communication
- Coordinating meetings with clients and cross-functional teams
- Supporting internal communication and report distribution
- Providing technical support for IRT systems and escalating issues when needed
Process Improvement & Team Support
- Contributing to improvements in IRT and Clinical Data Management processes
- Collaborating with departments such as:
- Clinical Operations
- Biostatistics
- Supply Chain
- Supporting training initiatives and knowledge-sharing activities
Eligibility Criteria
Educational Qualification
Candidates should have:
- B.Pharm / M.Pharm / Pharm.D
- B.Sc / M.Sc (Life Sciences)
- Diploma or equivalent qualification in healthcare or related fields
Experience Required
- 1 to 3 years of experience in:
- Clinical research
- Clinical data management (CDM)
- IRT systems or trial coordination
Skills Required
- Strong understanding of:
- Clinical trial processes and protocols
- IRT systems (randomization, drug supply, data capture)
- ICH-GCP and GxP guidelines
- Experience in:
- UAT testing and validation
- eTMF documentation systems
- Excellent communication and coordination skills
- Ability to manage timelines and multiple tasks
- Strong attention to detail and problem-solving ability
- Ability to work with global teams across time zones
Preferred / Additional Skills
- Knowledge of drug supply chain and labeling workflows
- Familiarity with clinical trial randomization processes
- Experience with IRT tools and reporting systems
- Exposure to system integrations and clinical data transfers
Salary & Benefits
- Estimated Salary: ₹4,50,000 – ₹8,00,000 per annum
- Additional benefits include:
- Remote work flexibility
- Exposure to global clinical trials
- Learning opportunities in IRT and advanced clinical systems
- Career growth in clinical operations and data management
Selection Process
The hiring process may include:
- Application screening
- HR interview
- Technical/functional interview
- Final selection
How to Apply
Interested candidates should apply through the official online application link provided by the company.
- Ensure your resume highlights experience in clinical research or IRT systems
- Apply early as positions may close quickly
Important Dates
- No fixed deadline mentioned
- Early application is recommended
Why Apply for This Pharma Job?
This role offers a strong foundation in clinical research technology and operations. Key benefits include:
- Opportunity to work on global clinical trials and IRT systems
- Gain expertise in randomization, drug supply, and eTMF systems
- Work remotely with international teams
- Build a future-ready career in clinical data and trial technology
- Exposure to CRO environment and advanced clinical tools
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform. We are not affiliated with Alimentiv or any recruiter. We do not charge any fees for job applications. Candidates are advised to verify all details from the official website before applying.
Final Call-to-Action
If you have experience in clinical research or data management and want to work in a high-growth, remote role, apply now and advance your career in clinical trial technology.
