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Consulting Project Manager

MSI Pharma
Bristol
4 weeks ago
Applications closed

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We’re Hiring: 1 x Programme Manager & 1 x Project Manager - GxP Software End-To-End Implementation


Please only apply if you have experience in consulting/advisory services.


Strong background in consulting/advisory services providing client-facing services i.e. SaaS solutions

Applicants need to be based in the United Kingdom, Croatia, Germany or Denmark ideally.

Proven experience of managing PV, Clinical, Regulatory and Quality technology projects.


1X Consulting Programme Manager


You will oversee multiple complex, cross-functional projects as part of large-scale programmes for Life Sciences clients. This a strategy focused role for someone experienced in managing multiple workstreams across software implementation.


Key Responsibilities:

  • Deliver enterprise-wide PV tech programmes across global pharma clients
  • Govern timelines, risks, budgets, and stakeholder expectations
  • Mentor project managers and drive delivery best practices
  • Lead engagements with executive stakeholders and client sponsors
  • Ensure compliance with GVP, GDPR, FDA/EMA, and other regulatory frameworks


Required Experience:

  • 12+ years in project/programme management (client-facing)
  • Strong background in consulting/advisory services (not pharma sponsor-side)
  • Proven track record of delivering safety, regulatory, or PV system programmes
  • Deep understanding of pharmacovigilance processes and tech platforms (e.g., Argus, ARISg)


1X Consulting Project Manager


You will manage end-to-end implementation of PV software solutions for Pharmaceutical clients, acting as the primary delivery contact and project lead.


Key Responsibilities:

  • Lead client-facing implementation and upgrade projects
  • Manage project plans, budgets, and delivery teams
  • Own stakeholder communication and risk management
  • Ensure compliance with regulatory and data privacy standards
  • Collaborate with internal consultants, third parties, and tech teams


Required Experience:

  • 8+ years in project management, including 5+ in life sciences tech
  • Background in a consultancy or advisory firm delivering PV/Regulatory projects
  • Familiarity with case management and safety systems (ex. Argus, ARISg)
  • Strong gasp of ICH E2E, GVP Modules, FDA/EMA standards


What we're looking for (Both Roles):


  • Consulting/Advisory experience is essential -candidates must have worked in a client-facing delivery-focused capacity
  • Strong understanding of GxP end-end systems, compliance, and tech delivery
  • Experience working with cross-functional, international teams
  • Excellent communication and stakeholder management skills
  • Danish speaking desirable


What’s On Offer:


  • Competitive salary
  • Remote-first work setup
  • A collaborative and fast-paced delivery environment
  • Global project scope with major pharmaceutical clients
  • Opportunity to drive digital innovation in drug safety

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