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HEOR Project Manager - 3+ Month Contract Pharmaceutical Services - Remote, US

Slipstream Life Sciences
United StatesRemotefull_timeVerifiedPosted 18 Feb 2026
💰 $240,000/yr($230,000/yr$240,000/yr)

About the role

Introduction

At Slipstream IT we work to streamline IT Support and provide managed solutions with a strategic consulting and global leadership management approach. Our solutions are designed exclusively for emerging pharma and biotech organizations.

Slipstream’s industry-leading solutions free clients from the demands of internal IT and allow them to rapidly advance their mission. Led by a leadership team that has been together for over 10 years, you will join a proven team, culture, and strategy to drive innovation within the IT outsourcing industry while developing your skillset with the opportunities for internal growth.

Responsibilities

  • Publications
    • Vendor, HCP, and cross-functional coordination:
      Liaise with external vendors, HCPs, and Servier cross-functional teams to support agency requests and ongoing collaboration.
    • Contracting and financial operations:
      Support Project Owner with contracting across agencies and HCP consultants/authors, including PO creation in NetSuite and coordination with Servier Finance, Cost Center Owner, and agencies on routine Finance exercises and reforecasting.
    • Project and timeline management:
      Manage timelines and deliverables across team activities, including meeting follow-up and documentation of action items from cross-functional working meetings.
    • Leadership reporting and communications:
      Complete quarterly metrics reporting by gathering inputs from functional area leads, updating slides, and providing cross-functional status updates, as needed.
    • Systems and operational support:
      Provide routine iEnvision “housekeeping” and support Veeva submissions for in-house developed materials (record creation, tagging/linking, MSRC grid completion), where needed.
    • Field Medical enablement and deployment:
      Coordinate with IT on deployment of new Field Medical materials and maintain the team materials tracker.
    • Other services:
      Additional support as mutually agreed between the Parties.
  • HEOR
    • Develop and submit RWE study concepts in collaboration with HEOR Strategy Leads for internal endorsements.
    • Study contracting and execution:
      Liaise with external vendors, and Servier cross-functional teams (Medical, Legal, Compliance, etc) to execute the study.
    • Contracting and financial operations:
      Support Project Owner with contracting across agencies and HCP consultants/authors, including PO creation in NetSuite and coordination with Servier Finance, Cost Center Owner, and agencies on routine Finance exercises and reforecasting.
    • Project and timeline management:
      Manage timelines and deliverables across team activities, including meeting follow-up and documentation of action items from cross-functional working meetings.
    • Leadership reporting and communications:
      Complete quarterly metrics reporting by gathering inputs from functional area leads, updating slides, and providing cross-functional status updates, as needed.

Qualifications

  • Minimum 6-10 Years pharmaceutical publication management and HEOR business analysis.
  • Proven successful project management work experience in a regulated pharmaceutical, biotech, or life sciences environment with deep ERP/validation knowledge is required.
  • Hands-on experience developing and maintaining project plans, dashboards, and trackers to drive accountability and transparency.
  • Proven ability to manage multiple (8–10) concurrent studies in a fast-paced, matrixed environment.
  • Technical Knowledge:
    • Must have direct experience using iEnvision, by Envision Pharma Group is a comprehensive, web-based platform designed to support the strategic and operational needs of medical affairs.
    • Must have direct experience in executing and managing Veeva submissions.
    • Familiarity with pharmaceutical RWE processes, data and systems is required.
    • Understanding of system development life cycle (SDLC) and computer software validation (CSV) methodologies.
  • Excellent Microsoft Office computer skills (Word, Excel, PPT, Visio, Onenote).
  • Excellent analytical and problem-solving skills, strong written and verbal communication, attention to detail, and the ability to manage relationships and influence stakeholders across departments.
  • Ability to present concepts and lead discussions on design issues with authority and poise both internally and to clients. This is a leadership-facing role.

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Company

Slipstream Life Sciences

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