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Program Leader

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Onsite

Program Leader

Cognizant Life Sciences Manufacturing

Program Leader

Skills

Performance Management

18 days ago

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Important information


Contract type:

Permanent

Location:

United Kingdom

Work mode:

Onsite

Published on:

2 October 2026

What they need


Enterprise MDR & CDR SaaS Implementation Programme | Cognizant Systems Integration

Hybrid — Remote (aligned to client hours) | GxP High

About the Role

Own end-to-end delivery, financial performance, resourcing, and stakeholder management for a multi-year enterprise MDR & CDR SaaS implementation programme, coordinating a 20+ person delivery team across CDR, MDR, Integration, and Validation workstreams.

Key Responsibilities

  • Own the programme plan, milestones, and RAID log across all workstreams

  • Chair weekly programme status forums with client IT/SIT/Business stakeholders

  • Resolve cross-workstream dependencies and ownership ambiguity

  • Own resourcing: attrition/backfill planning, performance management, team stabilisation

  • Own commercial health: burn, forecast-to-actual variance, change requests against SOW

  • Act as primary escalation point for client leadership; manage with structured RCA and action plans

  • Own programme-level accountability for the LSH-to-CDS migration cascade (MDR Lite → TCS MDR → CDS)

  • Own the programme risk register and audit/validation readiness (GxP traceability)

What You Bring

  • 12+ years programme/project management, incl. 5+ years leading large-scale, multi-workstream tech/SaaS programmes in regulated environments

  • Experience owning programme P&L, SOW/commercial governance, and change control

  • Proven multi-workstream delivery ownership (technical, functional, commercial)

  • Strong stakeholder/escalation management at senior/executive level

  • Workforce management at scale (attrition, performance, stabilisation)

  • GxP/regulated-industry experience; familiarity with validation lifecycle (URS, OQ/PQ)

  • Familiarity with clinical data platforms (CDR, MDR, EDC, LSH, or equivalent)

Desirable

  • Large pharma/regulated clinical data transformation programme experience

  • Familiarity with Medidata (Rave, CDS), TCS DO Accelerate, or equivalent

  • CDISC standards knowledge (USDM, SDTM, ADaM)

  • Legacy-to-SaaS coexistence/migration programme experience

  • PMP, PRINCE2, Agile/SAFe certification

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