Job Summary :
We are looking for an experienced Implementation Consultant to support the successful product deployments in the pharmaceutical and clinical trial domain . The ideal candidate will have a deep understanding of clinical trial processes, EDC / CTMS / IRT systems, and data management , ensuring seamless implementation, configuration, and support for customers.
Key Responsibilities : Product & Process Expertise
- Stay up-to-date with all clinical product features and releases .
- Analyze and understand current business processes, events, and data flows .
- Understand the impact of process changes and align them with business requirements.
- Act as a Clinical Subject Matter Expert (SME) , providing guidance to project teams.
- Write and document business requirements , translating them into functional solutions.
Implementation & Client Engagement
Lead client engagements to guide them through release planning and implementation efforts .Manage communication across internal teams, stakeholders, and customers .Ensure high-quality project deliverables, tracking status, risks, and issues.Oversee data mapping specifications for Saama Data Review Models .Act as a client liaison , collecting feedback and ensuring timely issue resolution.Support User Acceptance Testing (UAT) , assisting in configuration changes and issue triaging .Ensure a smooth transition from implementation to support.Analytics & Reporting
Provide advanced analytical and reporting support for various projects.Identify and define new sources of relevant clinical data for integration.Conduct data analysis and provide actionable recommendations .Support configuration quality checks to ensure solutions meet business objectives.Required / Must-Have Skills :
Experience in the pharmaceutical industry is essential .Strong knowledge of one or more clinical systems , including :EDC Systems (e.g., Medidata Rave, Veeva EDC, Oracle Clinical, Medrio, InForm).CTMS Systems (e.g., Siebel CTMS, Medidata CTMS, Veeva CTMS).IRT Systems (e.g., YPRIME, Parexel ClinPhone).Lab Systems (e.g., Central Labs, Local Labs).Good understanding of clinical trial processes, EDC study setup, and reporting workflows .Bachelor's or master's degree in healthcare , Computer Science, Engineering, or a related field .3-5 years of experience as a Product Manager or 1-2 years as a Product Owner .Experience working in an Agile environment .Good-to-Have Skills :
Familiarity with Software Development Life Cycle (SDLC) .Understanding of FDA regulations (21 CFR Part 11, GxP) .Experience working on multiple product life cycles .Technical knowledge of software development and web-based applications .Experience with healthcare software applications , particularly clinical systems.Why Join Us?
Work on cutting-edge clinical data and analytics solutions .Collaborate with a highly skilled pharmaceutical and clinical research team .Competitive salary, career growth opportunities, and exposure to leading life sciences technologies .If you are passionate about clinical data, implementation, and digital transformation , we encourage you to apply!