Jobs and Careers
SL

Pharma Project Manager, Level I - Remote, United States

Slipstream Life Sciences
Remote, United States, PA, United StatesRemotefull_timeVerifiedPosted 31 Jul 2026
💰 $85,000/yr($75,000/yr$85,000/yr)

About the role

At Slipstream 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.

Job Summary

The Pharma Project Manager, Level I plans, organizes, and executes projects that use data to create value. They lead teams through the project lifecycle, from development to operations, and are responsible for the project's success. Coordinates team across multiple departments and vendors for multiple concurrent projects.

Responsibilities

  • Project planning: Create and maintain project charter, roadmaps, timelines, and objectives. Manage project scope, schedule, financials and relationships.
  • Team management: Coordinate tasks, schedule and evaluate team members and manage stakeholder expectations
  • Project execution: Ensure projects meet timelines and resource constraints, and comply with legal and ethical requirements
  • Communication: Manages overall project communications including executive stakeholders, colleagues, vendors, business stakeholders, and clients as needed.
  • Documentation: Create and manage all project related artifacts including but not limited to Project Plans, RAID logs, Change Management, Status and Meeting documentation.
  • Risk management: Identify and manage project-related risks. Ensure appropriate escalations and mitigations.
  • Process improvement: Identify opportunities to improve operational efficiencies.
  • Vendor management: Manage contracts with vendors and suppliers.
  • Data project managers should have strong analytical and problem-solving skills and be able to work under pressure. They should also be able to multitask and guide and motivate others.
  • Work Pace: Ability to excel in a fast-paced, dynamic environment with multiple concurrent assignments.

Qualifications

  • Degree in life sciences or computer sciences or a related field strongly desired.
  • Must have relevant Information Technology pharmaceutical / biotechnology industry experience.
  • Minimum 5-7 Years commercial pharma/ biotech IT project management specifically in IT systems, data management, data warehousing and master data management.
  • Strong base understanding of standard data warehouse designs elements such as data ingestion, modification, and extraction.
  • Ability to articulate complex concepts in a simple and coherent manner, both verbally and in writing.
  • Proven experience of working with complex integrated systems, using creative and strategic thinking to deliver exceptional results.
  • Strong ability to listen to discussions and capture actions and requirements in meaningful, precise manner that can be understood by both technical and non-technical participants.
  • Ability to present concepts and lead discussions on design issues with authority and poise both internally and to clients. This is a client-facing role.
  • Ability to collaborate and relate to team members from a large variety of backgrounds on a daily basis. Must have experience working with local and virtual teams.
  • Excellent Microsoft Office computer skills (Word, Excel, PPT, Visio). Proficient with MS Project, Smartsheet, JIRA and common Microsoft Office applications (e.g., Excel, Power Point, Word, One Note, Visio, Outlook).
  • Experience working with SharePoint (or similar) project workspaces / document repositories.
  • Experience with the following items:
    • Working in a regulated environment, must have life sciences experience.
    • Working with and managing third party suppliers/vendors
  • Ability to operate with limited oversight and needs to command the respect of a broad range of business and technology stakeholders.
  • Ability to manage multiple projects simultaneously.
  • Proficient at recognizing and defining risks and developing response and mitigation plans for them.
  • Experience managing Commercial Off the Shelf (COTS) and / or Software as a Service (SaaS) projects, including integrations into and out of these systems, & data migrations.

Work Schedule

  • Typical schedule will be Monday to Friday, 8:00 AM to 5:00 PM.
  • Must be flexible to accommodate depar

Apply for this role

Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.

Apply Now →Generate Application Kit

Free account required — sign up in 30s

Company

Slipstream Life Sciences

View company profile →