Senior IT Technical Analyst, Clinical Systems

Role Summary

Senior IT Technical Analyst, Clinical Systems responsible for owning and advancing the portfolio of Clinical IT applications. Serves as the primary technology partner to Clinical Operations, Patient Supply, and Biostatistics teams to ensure systems are reliable, compliant, scalable, and aligned with scientific and operational goals. Plays a key role in implementing new modules and providing ongoing operational support, including requirements definition, solution design, configuration, documentation, testing, and integration. Balances strategy with hands-on execution to anticipate future needs and drive scalable solutions.

Responsibilities

• Act as the primary liaison between Clinical teams and IT.
• Lead the implementation, enhancement, and support of Clinical IT systems.
• Shape the clinical systems landscape in partnership with Clinical stakeholders and IT leadership. Manage system roadmap development, evaluation and selection of new technologies, and integration of relevant systems.
• Gather and document business requirements and ensure these are translated into high quality technical solutions that meet the needs of our organization.
• Lead continuous improvement efforts for existing systems. Partner closely with business stakeholders to collect and prioritize enhancement requests. Stay up to date on new technologies and best-practices and make recommendations for potential improvements.
• Support validation and change management activities, including contributing to requirements documentation, test scripts, and change control documentation.
• Serve as primary operational support to resolve any system related issues.
• Support the larger IT organization by assuming other duties and responsibilities, as assigned.

Qualifications

• 6+ years of experience implementing IT systems within the life sciences industry.
• Demonstrated experience with and strong understanding of one or more Clinical systems (IRT/RTSM, eTMF, CTMS, SAS, clinical dataset generation and validation).
• Strong understanding of Computer Systems Validation (CSV), GxP, and 21 CFR Part 11regulations.
• Excellent communication, facilitation, and stakeholder‑management skills.
• Proven ability to lead cross‑functional initiatives and manage vendors.
• Onsite requirements: Candidates are expected to come onsite 2 days per week and as needed to complete job duties.