Planview & Integration Developer

At Clario, part of Thermo Fisher Scientific, The Planview & Integration Developer plays a key role in shaping and scaling Clario’s enterprise project portfolio management and integration ecosystem. This role supports the configuration, support, and continuous improvement of our global Planview Portfolios (Enterprise One) platform and enterprise integrations, enabling high‑impact decision‑making across the business. Designed for an early‑career technologist eager to accelerate their growth, this position offers hands‑on experience with industry‑leading PPM tools, real‑world enterprise integrations, and validated systems within a global, regulated life‑sciences environment. You’ll work alongside experienced professionals, gain exposure to complex enterprise ecosystems, and build skills that are highly transferable across modern digital organizations. What We Offer Competitive compensation Provident Fund & Gratuity Flexible leave plans Engaging employee programs Hybrid work environment What You’ll Be Doing Planview Platform & Integrations Support day‑to‑day administration of the Planview Portfolios (Enterprise One) platform Assist with configuration and maintenance of Planview modules under senior guidance Support development, testing, and maintenance of integrations with systems such as Workday, Jira, Oracle EBS, and the Enterprise Lakehouse Foundation (ELF) Help build and maintain basic APIs, scripts, data connections, and scheduled jobs Participate in troubleshooting system, integration, and data issues Development, Testing & Operations Assist with system configuration, deployments, enhancements, and defect fixes Participate in functional, integration, and regression testing cycles Support routine maintenance and operational activities across environments Reporting & Data Support Assist in developing and maintaining reports, dashboards, and extracts using SSRS, Power BI, or Planview tools Perform data validation and reconciliation to support accurate portfolio, time, and financial reporting Support ad‑hoc reporting and analysis requests from PMO, Finance, and business teams Documentation, Compliance & Collaboration Support preparation of technical documentation, including requirements, test plans, and validation artifacts Learn and apply SDLC, change control, and validation practices to maintain system compliance Work with PMO, IT, Finance, Product, and vendors to understand business needs Communicate progress, risks, and issues clearly within project and operational forums Actively participate in training, mentorship, and continuous learning What We Look For Bachelor’s degree in Computer Science, Engineering, or a related field (or equivalent experience) Early‑career experience through academic projects, internships, or professional roles Strong interest in Planview Enterprise One, system integrations, and enterprise platforms Working knowledge of SQL and relational databases Exposure to reporting or BI tools such as SSRS or Power BI Understanding of the software development lifecycle (SDLC) Clear technical documentation and communication skills in English Analytical mindset and ability to work effectively in a team environment Exposure to regulated environments is a plus, but not required At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you’re starting your clinical data career or building long‑term expertise, your work helps bring life‑changing therapies to patients faster. Clario Privacy Policy Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.