Job Opportunity: IRT Coordinator (Remote, India)

Job Summary

Alimentiv is seeking a detail-oriented and motivated IRT (Interactive Response Technology) Coordinator to join our global clinical trial operations team. This remote position is designed for professionals with 1–3 years of experience in clinical research, data management, or IRT systems who are eager to advance their careers in a high-growth CRO environment. As an IRT Coordinator, you will play a vital role in ensuring the integrity of clinical trial randomization, drug supply logistics, and regulatory compliance. If you are passionate about clinical data systems, User Acceptance Testing (UAT), and cross-functional project coordination, we invite you to apply and contribute to our mission of advancing global health.

Key Responsibilities

Clinical Trial & IRT Project Support

• System Lifecycle Management: Assist in the administration and documentation of IRT systems throughout the entire trial lifecycle, from project start-up through to study maintenance and close-out.
• Documentation & Testing: Draft essential IRT user guides, develop UAT scripts, and maintain rigorous test documentation. Lead and support UAT and database validation efforts to ensure system accuracy.
• Logistics & Inventory: Oversee drug inventory tracking and streamline ordering processes to ensure site readiness.
• Data & Reporting: Generate, review, and distribute clinical trial reports. Manage clinical data transfers and maintain accurate records within the electronic Trial Master File (eTMF).
• Technical Support: Serve as a point of contact for user support, resolving issues and facilitating escalations as required.
• Collaboration: Coordinate client meetings, prepare internal communications, and actively engage in cross-functional discussions to ensure project milestones are met.

Operational & Departmental Support

• Process Improvement: Proactively identify and contribute to improvements in IRT and Clinical Data Management (CDM) workflows.
• Cross-Functional Partnership: Collaborate effectively with Clinical Operations, Biostatistics, and Supply Chain departments.
• Compliance & Excellence: Promote adherence to ICH-GCP, GxP, and internal regulatory standards. Participate in internal training and knowledge-sharing initiatives to maintain high operational standards.

Requirements

• Education: A diploma or degree in Life Sciences, Pharmacy, or a closely related field.
• Experience: 1–3 years of hands-on experience in clinical research, IRT administration, Clinical Data Management (CDM), or trial coordination.
• Technical Proficiency:
  • Solid understanding of clinical trial protocols, randomization procedures, drug supply chains, and data capture processes.
  • Proven experience with UAT testing, User Requirement Specifications (URS), and validation procedures.
  • Familiarity with eTMF systems and clinical documentation standards.
• Soft Skills: Exceptional communication and coordination skills. Ability to manage multiple projects and timelines in a fast-paced, remote environment.
• Collaborative Mindset: Demonstrated ability to work successfully with global teams across different time zones.

Benefits

• Competitive Compensation: An estimated salary range of ₹4,50,000 – ₹8,00,000 per annum, commensurate with experience.
• Remote Work Environment: Enjoy the flexibility of working remotely from anywhere in India.
• Professional Development: Gain invaluable exposure to advanced IRT systems, eTMF, and high-stakes global clinical trials.
• Career Growth: A clear pathway to advance your expertise in Clinical Data Management and Clinical Operations within an internationally recognized CRO.
• Impactful Work: Participate in cutting-edge clinical research that makes a tangible difference in patient lives.

How to Apply

If you are a dedicated professional looking to grow your career in clinical research technology, we would love to hear from you. Please submit your application via the official company portal link provided below:

[Link to Application Portal]

Alimentiv is an equal opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees.