--- title: 'UAT Tester at Endpoint Clinical' canonical: 'https://feeny.ai/job/uat-tester-endpoint-clinical-bengaluru-n7z3aehx61bf' type: 'job' last_seen: '2026-09-10' --- # UAT Tester at Endpoint Clinical - **Company:** Endpoint Clinical - **Location:** Bengaluru, India - **Employment:** full-time - **Work type:** onsite - **Posted:** 2026-06-24 - **Last confirmed live:** 2026-09-10 - **Apply:** https://jobs.lever.co/endpointclinical/5cb3591d-b562-43b3-bc6a-69d5cb568f77 ## Job description About Us: Endpoint is an interactive response technology (IRT®) systems and solutions provider that supports the life sciences industry. Since 2009, we have been working with a single vision in mind, to help sponsors and pharmaceutical companies achieve clinical trial success. Our solutions, realized through the proprietary PULSE® platform, have proven to maximize the supply chain, minimize operational costs, and ensure timely and accurate patient dosing. Endpoint is headquartered in Raleigh-Durham, North Carolina with offices across the United States, Europe, and Asia. Position Overview: The UAT Tester for RTSM (Randomization and Trial Supply Management) Systems will be responsible for planning, designing, executing, and documenting User Acceptance Testing activities for RTSM solutions used in clinical trials. This role ensures that systems meet user requirements, function as expected, and are compliant with applicable regulatory and quality standards (e.g., GxP, 21 CFR Part 11). The role is available at our offices in Bangalore. Responsibilities: - Collaborate with sponsor stakeholders and project teams to define UAT scope, scenarios, and acceptance criteria. - Develop UAT test plans, scripts, and data based on functional requirements and study protocols. - Execute test cases, document results, and track defects to closure in coordination with the sponsor and internal stakeholders. - Validate randomization schemes, drug supply logic, visit schedules, and site management features specific to the RTSM system. - Participate in UAT readiness and kick-off meetings, walkthroughs, and test script reviews. - Ensure system behavior aligns with end-user expectations across diverse use cases including subject enrollment, kit management, unblinding, resupply triggers, and shipment tracking. - Maintain clear and audit-ready UAT documentation, including traceability matrices, deviation logs, and summary reports. - Support study teams during go-live readiness activities and contribute to lessons learned for future system deployments. - Work closely with Quality, Trust and Compliance team to ensure testing adheres to applicable SOPs, validation standards, and regulatory guidelines. Education: - Bachelor’s degree in Life Sciences, Computer Science, Information Technology, or a related field. Experience: - 2–5 years of experience in User Acceptance Testing or Validation of Clinical Trial systems, ideally RTSM/IWRS/IRT platforms. - Familiarity with clinical trial processes, ICH-GCP, and regulatory requirements (e.g., 21 CFR Part 11, EU Annex 11). - Strong understanding of subject randomization and drug supply strategies. - Detail-oriented with excellent documentation, troubleshooting, and communication skills. - Proficient in defect tracking and test management tools (e.g., JIRA, SpiraTeam, Azure DevOps). - Ability to meet deadlines and work under pressure. - Demonstrates flexibility and adaptability to shift gears according to the priority of tasks. Possesses a high degree of flexibility, accountability, and responsibility. - Capacity to work independently once given adequate instructions. - Communication – Proficient verbal and written communication skills. Willingness to share and receive information and ideas from all levels of the organization in order to achieve the desired results. Ability to compose clear, concise, and professional written communication. - Teamwork – Commitment to the successful achievement of team and organizational goals through a desire to participate with and help other members of the team. Skills: - Strong collaboration and development skills. - Proactive team player enthusiastic with high work ethics #LI-MT #LI-Onsite ## About Endpoint Clinical ## Company Overview - **One-liner**: Endpoint Clinical provides Randomization and Trial Supply Management (RTSM) technology and services to clinical trial sponsors and CROs, helping them manage complex global trials efficiently. - **Entity Type**: Private - **Headquarters**: Raleigh, North Carolina, United States - **Founded**: 2009 - **Founders**: Not publicly available ## Core Business - **Primary industry/industries**: Life Sciences / Clinical Trial Technology (RTSM/IRT) - **Target customers**: B2B – Biopharmaceutical companies (from emerging biotech to 8 of the Top 15), Contract Research Organizations (CROs) - **Mission or purpose statement**: To help set the foundation for clinical trial success by delivering innovative, high-quality RTSM solutions that make a difference in advancing lifesaving treatments. ## Products & Services - **[PULSE®]**: A fully customizable and adaptive dynamic RTSM platform designed to scale with trial workflow and deliver real-time responsiveness for evolving needs. (SaaS/Platform) - **[Elosity]**: A multi-tenant, robust RTSM platform offering enhanced speed, flexibility, and AI-driven capabilities to optimize trial logistics and patient outcomes. (SaaS/Platform) - **RTSM Support & SLAs**: Proactive, expert-led support with defined service level agreements to keep trials running smoothly. (Service) - **AI Services**: Harnessing AI-driven insights to streamline eClinical operations and enable smarter decision-making across global trials. (Service) - **UAT Services**: Comprehensive, independent User Acceptance Testing to ensure flawless RTSM performance and accelerate study timelines. (Service) - **Consulting Services**: Expert consulting on randomization and drug supply strategies to enhance trial integrity and optimize resource allocation. (Service) ## Market Standing - **Valuation/Market Cap**: Not publicly available - **Key Metric**: Annual Revenue of **$65.6M** (estimated) [linkedin.com] - **Total Funding**: **$1.7M** [linkedin.com] - **Notable Investors/Partners**: Not publicly disclosed. Partners with 300+ sponsors including 8 of the Top 15 Biopharma leaders [endpointclinical.com]. - **Growth Signals**: - Recognized as an **RTSM Leader** in the Everest Group 2025 PEAK Matrix® Assessment [endpointclinical.com]. - Powers trials across **90+ countries** and works with **100,000+ clinical trial sites** [endpointclinical.com]. - Has supported **over 1M patients** across **2,000+ clinical studies** [endpointclinical.com]. - Headcount of **~486-600 employees**, with a modest growth of 0.5% YoY [linkedin.com, endpointclinical.com]. ## Competitive Advantages - **Deep RTSM Expertise**: Nearly 20 years of RTSM advancement and 200+ years of combined industry experience on the leadership team [endpointclinical.com]. - **Proven Scale & Reliability**: Demonstrated ability to support complex, adaptive trials across a wide range of therapeutic areas (20+) including oncology and rare diseases [endpointclinical.com]. - **Governance-First Approach**: Built-in controls, audit readiness, and regulatory alignment provide a strong quality and compliance mindset [endpointclinical.com]. - **Leadership Recognition**: Named a Leader by the Everest Group, a highly respected industry analyst firm [endpointclinical.com]. ## Strategic Focus - **Innovation & AI**: Integrating AI-driven capabilities into platforms (Elosity) to optimize trial logistics and improve patient outcomes [endpointclinical.com]. - **Global Expansion**: Continuing to support trials globally across 90+ countries [endpointclinical.com]. - **Operational Excellence**: Maintaining a strong focus on quality, compliance, and proactive support as key differentiators [endpointclinical.com]. ## Why Work Here - **Culture**: Endpoint Clinical emphasizes a culture of excellence, accountability, and collaboration. They want to be a "top career destination" [endpointclinical.com]. - **Awards**: Recognized by Built In as a **Top 100 Midsize Place to Work** from 2021 to 2025 [endpointclinical.com]. - **Work Policy**: Employs a **hybrid** work model with flexible on-site expectations. Offices are located globally including the US (Raleigh, MA), Europe, and Asia [builtin.com, endpointclinical.com]. - **Global Team**: A workforce of over 600 people spread across 10 countries (including India, US, UK, Philippines, China), fostering a collaborative, global culture [linkedin.com, endpointclinical.com]. - **Benefits**: Offers performance bonuses, generous parental leave, family medical leave, dental insurance, Flexible Spending Account (FSA), and customized development tracks [builtin.com]. - **Engineering & Innovation**: The company is focused on next-generation technology and AI, indicating a dynamic and challenging environment for technical talent [endpointclinical.com]. - **Note on Employee Sentiment**: The current employee rating on LinkedIn is 2.9/5.0 (based on 177 reviews), with culture and career opportunities rated lower (2.5/5.0) [linkedin.com]. This is an important data point to consider. ## Sources 1. [endpointclinical.com](https://www.endpointclinical.com/) 2. [endpointclinical.com - Careers](https://www.endpointclinical.com/careers) 3. [endpointclinical.com - Company](https://www.endpointclinical.com/company) 4. [linkedin.com](https://linkedin.com/company/endpoint_464541) 5. 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