Principal Technical Project Manager
eClinical SolutionsUnited States
Posted August 28, 2025
Full Time
About the Company
eClinical Solutions is a leading provider of data & analytics platforms and biometrics services for biopharma researchers. Their elluminate® platform enables efficient clinical trial management, offering accurate insights to reduce cycle times and improve productivity. With expertise in areas like clinical data management, statistical programming, and risk-based quality management, eClinical stands out for its comprehensive solutions and global workforce.
Job Description
eClinical Solutions is seeking a Principal Technical Project Manager to deliver high-quality products and services to life science clients and partners. This role focuses on overseeing the successful delivery of eCS' elluminate platform, a next-generation data integration and analytics cloud, and supporting technical projects involving solution integration, custom reporting, data mapping, and CDR management. The project manager will drive project adoption, foster client relationships, and mitigate risks in a fast-growing company.
Requirements
- Bachelor's degree preferred, in a health sciences or analytic discipline
- Project Management Professional (PMP) certification or in process preferred
- 10+ years of project management experience preferably in a clinical, biomedical, or software environment
- 5+ years in Pharmaceutical/Biotechnology industry or equivalent senior consulting role managing large complex clients/multiple projects
- Experience managing employees desired
- Experience independently identifying and implementing process efficiencies and quality improvements within the PMO
- Experience setting operational standards and best practices for eCS project management services
- Expertise in Microsoft applications and collaborative platforms (MS Teams, OneDrive, SharePoint)
- Knowledge of PMI and industry best practices
- Experience managing projects focused on technical deployments, system implementations, and data management
- Working knowledge and commitment to ICH/GCP guidelines, 21 CFR Part 11, clinical trials methodology, CRO partnerships, EDC systems
- Working knowledge of 21 CFR Part 11
- Working knowledge of ICH/GCP guidelines, 21 CFR Part 11
- Working knowledge of 21 CFR Part 11
- Working knowledge and experience with ICH/GCP guidelines, 21 CFR Part 11
- Working knowledge and experience with 21 CFR Part 11
- Working knowledge and experience with ICH/GCP guidelines, 21 CFR Part 11
- Experience independently identifying and implementing process efficiencies and quality improvements within the PMO
