Pharma IT Project Manager – GxP/R&D, Hybrid

Slipstream IT, LLC

Fall River (MA)

Vor Ort

USD 90.000 - 150.000

Vollzeit

Vor 5 Tagen
Sei unter den ersten Bewerbenden

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Zusammenfassung

Slipstream Life Sciences in Fall River, MA, is seeking a Contract Project Manager to lead IT initiatives across commercial, clinical, regulatory, and R&D domains. You will ensure projects meet scope, schedule, and budget while aligning with business objectives.

Approximately 30% of time is dedicated to GLP/GMP environments, supporting R&D IT partnerships and PMO maturation. On-site presence is required with some flexibility.

Qualifikationen

  • Bachelor’s degree in Computer Science, Information Technology, or related field.
  • 7+ years of IT experience with 3–5 years in project management.
  • 5+ years of experience in commercial pharma, biotech, or clinical research.
  • 2-5 years of experience in business analysis is preferred.
  • Experience in regulated environments (Pharma, Biotech, Clinical, Medical Device).

Aufgaben

  • Manage end-to-end project lifecycle for IT infrastructure, operations, and R&D technology initiatives.
  • Develop and maintain detailed project plans, including scope, schedule, budget, and risk management.
  • Lead cross-functional project teams across commercial, clinical, regulatory, and R&D domains.
  • Track project progress and provide regular status updates to stakeholders.
  • Conduct project status meetings and manage change control processes.
  • Spearhead process streamlining, training, audits, and KPI/metrics tracking.

Kenntnisse

Project management
GxP compliance
Smartsheet
JIRA
MS Project
Vendor management

Ausbildung

Bachelor’s degree in Computer Science, IT, or related field

Tools

Smartsheet
MS Project
JIRA

Jobbeschreibung

Slipstream Life Sciences in Fall River, MA, is seeking a Contract Project Manager to lead IT initiatives across commercial, clinical, regulatory, and R&D domains. You will ensure projects meet scope, schedule, and budget while aligning with business objectives.

Approximately 30% of time is dedicated to GLP/GMP environments, supporting R&D IT partnerships and PMO maturation. On-site presence is required with some flexibility.

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