IT Project Manager

Lancesoft; Nutley (NJ); On-site; USD 140,000 - 180,000; Full time

Job summary

Lancesoft in Nutley, NJ seeks a Senior IT Project Manager to lead global Clinical R&D technology initiatives from planning through validated implementation and handoff. You will partner with business, IT, Quality, Validation, Security, Architecture, and vendors, providing governance, reporting, and escalation as needed.

The ideal candidate brings senior project leadership in pharmaceutical, biotech, or CRO environments with a track record delivering regulated systems, data platforms, or

Qualifications

• 15+ years of professional IT experience, including 10+ years managing complex IT projects in pharmaceutical, biotechnology, or CRO environments.
• Demonstrated experience delivering global regulated Clinical R&D system implementations, migrations, upgrades, integrations, or modernization programs.
• PMP preferred; Agile, Scrum, SAFe, or equivalent certification is a plus.
• Strong knowledge of clinical R&D processes, regulatory guidelines, and data integrity.

Responsibilities

• Lead global, multi-workstream Clinical R&D IT projects through validated implementation and operational transition.
• Strategy, governance, and business alignment with reporting on progress, budgets, risks, and benefits.
• Stakeholder, vendor, and team leadership; manage contracts, SLAs, milestones, and cross-functional forums.
• Ensure compliance with GxP, CSV, SDLC, change control, testing, traceability, and audit readiness.

Skills

PMP certification

Agile / Scrum / SAFe

Executive communication

Risk management

Stakeholder leadership

Education

Bachelor's degree in IT, Computer Science, Life Sciences, Engineering, Business, or a related field

Job description

Role Summary

Senior IT Project Manager to lead global Clinical R&D technology initiatives from planning through validated implementation and operational handoff, with accountability for scope, schedule, budget, quality, risk, resources, and compliance. The resource will partner with business, IT, Quality, Validation, Security, Architecture, and vendors while providing governance, executive reporting, and timely escalation. Ideal profile: Senior project leader with pharmaceutical, biotechnology, or CRO experience delivering regulated clinical systems, data platforms, cloud solutions, integrations, migrations, or upgrades.

Scope of Responsibilities

• Project Delivery and Execution Lead global, multi-workstream Clinical R&D IT projects through validated implementation and operational transition. Maintain charters, integrated plans, schedules, budgets, resources, risks, issues, decisions, dependencies, and acceptance criteria. Control scope, timeline, cost, quality, benefits, and delivery commitments;coordinate technical workstreams and corrective actions.
• Strategy, Governance, and Business Alignment Define project outcomes, roadmap, governance, success measures, and delivery structure with business and IT leaders. Lead steering committees and decision forums;provide concise reporting on progress, financials, risks, issues, dependencies, and benefits. Maintain alignment with Clinical R&D priorities, technology strategy, compliance, and operational objectives.
• Stakeholder, Vendor, and Team Leadership Serve as the primary contact and escalation point for sponsors, stakeholders, IT teams, quality partners, and vendors. Lead cross-functional teams and global project forums;drive accountability and timely decisions. Manage vendors, contractors, contracts, statements of work, milestones, service levels, quality, and acceptance criteria.
• Compliance, Risk, Financial, and Change Management Ensure delivery meets GxP, CSV, data integrity, security, SDLC, change control, testing, traceability, release, and SOP requirements. Manage project, compliance, financial, vendor, resource, dependency, and operational risks. Track budgets, forecasts, spend, funding, and resource utilization. Support communication, training, adoption, transition, and audit‑ready documentation.

Candidate Requirements

Education and Experience Bachelor s degree in IT, Computer Science, Life Sciences, Engineering, Business, or a related field. 15+ years of professional experience, including 10+ years managing complex IT projects in pharmaceutical, biotechnology, or CRO environments. Demonstrated experience leading global regulated Clinical R&D system implementations, migrations, upgrades, integrations, or modernization programs. PMP preferred;Agile, Scrum, SAFe, or equivalent certification is a plus.

Industry and Technical Knowledge

• Strong knowledge of Clinical R&D processes, clinical data flows, and the clinical technology landscape.
• Working knowledge of GAMP 5, GCP, GDP, GDPR, 21 CFR Part 11, CSV, data integrity, SDLC, and release governance.
• Experience with Waterfall, Agile, and hybrid delivery;cloud, data, infrastructure, cybersecurity, and integration concepts.
• Strong executive reporting, business case, portfolio, resource, budget, and project planning skills.

Core Competencies

• Executive communication and stakeholder influence
• Strategic thinking and business acumen
• Risk management and problem solving
• Accountability, collaboration, and change leadership

Expected Outcomes

Projects delivered within approved scope, schedule, budget, quality, and compliance expectations. Effective governance, actionable reporting, and timely escalation. Validated solutions delivered with inspection‑ready documentation and a sustainable operational transition.