
Pharma Project Manager, Level I
Posted Aug 1

Posted Aug 1
This is a fully remote position, open to applicants in Pennsylvania.
• The Pharma Project Manager, Level I is responsible for planning, organizing, and executing projects that leverage data to generate value.
• They guide teams throughout the project lifecycle, from development to operations, ensuring the project's overall success.
• Coordinates teams across various departments and vendors for multiple concurrent projects.
• Project planning: Develop and maintain project charters, roadmaps, timelines, and objectives.
• Manage project scope, schedule, financials, and stakeholder relationships.
• Team management: Organize tasks, schedule, assess team members, and manage stakeholder expectations.
• Project execution: Ensure projects adhere to timelines and resource constraints, while complying with legal and ethical standards.
• Communication: Oversee all project communications, including those with executive stakeholders, colleagues, vendors, business stakeholders, and clients as required.
• Documentation: Create and manage all project-related artifacts, including but not limited to project plans, RAID logs, change management documents, status updates, and meeting records.
• Risk management: Identify and address project-related risks, ensuring appropriate escalations and mitigation strategies are in place.
• Process improvement: Discover opportunities to enhance operational efficiencies.
• Vendor management: Oversee contracts with vendors and suppliers.
• A degree in life sciences, computer sciences, or a related field is strongly preferred.
• Relevant experience in the Information Technology pharmaceutical/biotechnology industry is essential.
• A minimum of 5-7 years of commercial pharma/biotech IT project management experience, specifically in IT systems, data management, data warehousing, and master data management.
• A solid foundational understanding of standard data warehouse design elements, such as data ingestion, modification, and extraction.
• Capability to articulate complex concepts clearly and coherently, both verbally and in writing.
• Proven experience working with complex integrated systems, employing creative and strategic thinking to achieve outstanding results.
• Strong listening skills to capture actions and requirements in a meaningful and concise manner that is comprehensible to both technical and non-technical participants.
• Ability to present concepts and lead discussions on design issues with confidence and poise, both internally and with clients.
• This role is client-facing.
• Ability to collaborate effectively with team members from diverse backgrounds on a daily basis.
• Experience working with both local and virtual teams is required.
• Excellent skills in Microsoft Office applications (Word, Excel, PPT, Visio).
• Proficient with MS Project, Smartsheet, JIRA, and common Microsoft Office applications (e.g., Excel, PowerPoint, Word, OneNote, Visio, Outlook).
• Experience with SharePoint (or similar) project workspaces/document repositories.
• Experience working in a regulated environment; life sciences experience is essential.
• Experience managing third-party suppliers/vendors.
• Ability to operate with minimal oversight and earn the respect of a wide range of business and technology stakeholders.
• Capability to manage multiple projects simultaneously.
• Skilled at identifying and defining risks and developing response and mitigation plans.
• Experience managing Commercial Off the Shelf (COTS) and/or Software as a Service (SaaS) projects, including integrations into and out of these systems, and data migrations.
• 401k matching
• Comprehensive group health, dental, and vision benefits
• Life insurance and long-term disability (LTD)
• Discretionary paid time off (PTO)
Sigma Software Group
Thermo Fisher Scientific
Jeevan Technologies (a Nobl Q company)
Trilogy Federal
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