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Cognizant Life Sciences Manufacturing

Program Leader

United Kingdom
Posted about 21 hours ago
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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)

Reasons to use Rodeo

I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?

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Also worth knowing: most autumn 2026 applications are open now. Timing matters more than you think.

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Graduate Consultant — 2026 Scheme

PwC·London, UK
£35,000/yr

Why you're a good match

Strong

Your economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.

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It searches the market for you

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Why you're a good match

You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.

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Strong

Experience fit

Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.

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Strong

Only hits

No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.

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)

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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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Location

United Kingdom

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