eClinical Business Lead, UAT Lead in India at Jobgether

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for an eClinical Business Lead, UAT Lead based in India.

This role offers the opportunity to lead technology validation initiatives that support the delivery of innovative clinical research solutions.
The position focuses on managing User Acceptance Testing (UAT) for critical eClinical platforms, ensuring systems meet business, regulatory, and operational requirements.
You will collaborate with clinical teams, technology vendors, sponsors, and cross-functional stakeholders to deliver reliable digital solutions.
The role combines project leadership, technical understanding, quality assurance, and stakeholder management within a regulated environment.
You will contribute directly to improving clinical trial execution, patient safety, and the efficiency of research operations.
This is an ideal opportunity for professionals passionate about healthcare technology, clinical systems, and continuous process improvement.

The eClinical Business Lead/UAT Lead will oversee the planning, execution, and delivery of User Acceptance Testing activities for clinical trial technology platforms. The role requires strong coordination skills, technical awareness, and the ability to ensure quality outcomes across complex clinical technology implementations.

• Lead and manage UAT delivery for eClinical vendor systems, including IRT/RTSM, eCOA, ePRO, and system integrations.
• Define UAT plans, manage timelines, and ensure testing deliverables are completed according to project requirements.
• Review clinical protocols and technical documentation to identify appropriate test scenarios and create comprehensive test scripts.
• Analyze system requirements and collaborate with stakeholders to validate configurations and integration needs.
• Identify risks related to system setup, integrations, quality, timelines, and project delivery, implementing mitigation strategies when needed.
• Act as the primary UAT contact for project teams, vendors, and sponsors, maintaining strong stakeholder relationships.
• Coordinate testing resources, including testers and technical quality teams, to support successful execution.
• Ensure technology setup activities are accurately documented and aligned with project budgets.
• Support audit activities and maintain compliance with clinical research standards and documentation requirements.
• Train and mentor junior team members while contributing to team knowledge development.
• Stay informed about evolving clinical technology solutions, industry practices, and platform capabilities.
• Drive continuous improvement initiatives to enhance testing processes and clinical technology delivery.

The ideal candidate brings experience in clinical research technology, software validation, and stakeholder coordination, with the ability to manage complex priorities in a regulated environment.

• Bachelor’s degree in life sciences, computer science, information technology, or equivalent experience.
• 5+ years of experience in clinical research, clinical trial operations, CRO, pharmaceutical, healthcare, or related regulated environments.
• Proven experience with configuration, delivery, validation, or testing of clinical trial systems such as IRT/RTSM, eCOA, or ePRO.
• Experience creating test case scenarios, test scripts, and managing User Acceptance Testing activities.
• Knowledge of Good Documentation Practices (GDP) and electronic testing processes.
• Understanding of ICH-GCP, regulatory requirements, 21 CFR Part 11, and clinical trial processes.
• Strong project management, communication, organization, and problem-solving skills.
• Ability to interpret technical documentation and translate requirements into practical testing approaches.
• Experience collaborating with vendors, sponsors, and cross-functional teams.
• Ability to independently manage multiple priorities and lead meetings effectively.
• Fluent written and verbal English communication skills.

Preferred Qualifications:

• Experience designing, testing, or delivering IRT, eCOA, or ePRO solutions.
• Knowledge of clinical data standards such as CDISC SDTM.
• Experience mentoring team members and providing day-to-day guidance.
• Understanding of data standards and their application within clinical trial environments.
• Familiarity with clinical technology platforms and software testing methodologies.

• Flexible remote work opportunity.
• Opportunity to contribute to impactful clinical research technology projects.
• Career growth opportunities within a global healthcare environment.
• Continuous learning and professional development opportunities.
• Exposure to innovative eClinical platforms and digital health solutions.
• Collaborative work environment with multidisciplinary global teams.
• Opportunity to support projects that contribute to advancing patient-focused healthcare.