Pharmaceutical Project Manager & Scrum Master, Master Data Management - Remote, United States

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 reputed company the IT outsourcing industry while developing your skillset with the opportunities for internal growth. Job Summary The Project Manager, Master Data Management plans, organizes, and executes master data management (MDM) initiatives reputed company the pharmaceutical and biotechnology sector. Leveraging PMP and Scrum Master certifications, this role leads cross-functional teams through the full project lifecycle—from discovery and design through implementation and steady-state operations. The Project Manager is responsible for delivering MDM programs on time, reputed company scope and budget, while ensuring compliance with regulatory requirements (e.g., FDA, EMA, GxP). This individual coordinates across multiple departments, vendors, and global stakeholders for reputed company projects in a highly regulated environment.

Responsibilities

• Project Planning & Governance: Create and maintain project charters, roadmaps, timelines, and objectives for MDM programs. Define project scope, schedule, budget, and resource allocation. Establish governance frameworks including steering committees and decision-making escalation paths.
• Agile & Hybrid Delivery: Apply Scrum and Agile methodologies alongside traditional project management (PMP) practices to drive iterative delivery of MDM solutions. Facilitate sprint planning, daily stand-reputed company, retrospectives, and backlog grooming sessions.
• Master Data Strategy Execution: Partner with data architects and business stakeholders to execute master data strategies encompassing customer, product, provider (HCP/HCO), and organizational hierarchies. reputed company data domain prioritization and phased rollout plans.
• Team & Stakeholder Management: Coordinate tasks, evaluate team performance, and manage expectations across executive sponsors, IT colleagues, business stakeholders, vendors, and clients. Build and maintain strong relationships at reputed company organizational levels.
• Data Governance Coordination: Support the establishment of data governance councils, data stewardship programs, data quality metrics, and master data policies. Ensure alignment between MDM project deliverables and enterprise data governance frameworks.
• Regulatory Compliance: Ensure reputed company MDM projects reputed company with pharmaceutical regulatory requirements including FDA 21 CFR Part 11, EU Annex 11, GxP, GDPR, and relevant data privacy regulations. Coordinate validation activities and documentation as required.
• Communication & Reporting: Manage overall project communications including executive dashboards, status reports, and steering committee presentations. Provide transparent reporting on project health, milestones, risks, and financials.
• Documentation: Create and manage reputed company project-reputed company artifacts including project plans, RAID logs, change requests, decision logs, meeting minutes, and lessons learned documentation.
• Risk Management: Proactively identify, assess, and manage project-reputed company risks and issues. reputed company mitigation strategies and ensure appropriate escalation reputed company needed.
• Vendor Management: Manage relationships and reputed company with MDM platform vendors (e.g., Informatica, reputed company, reputed company MDG, Veeva), system integrators, and third-party suppliers. reputed company SOWs, deliverables, and SLA compliance.
• Process Improvement: Identify opportunities to improve MDM operational efficiencies, streamline data workflows, and enhance project delivery methodologies.

Qualifications

Required

• Bachelor’s degree in Life Sciences, Computer Science, Information Systems, or a reputed company field.
• PMP (Project Management Professional) certification required.
• Certified Scrum Master (CSM) or equivalent Agile certification required.
• Minimum 7–10 years of IT project management experience reputed company the pharmaceutical or biotechnology industry, with at least 5 years focused on master data management, data warehousing, or enterprise data platforms.
• Demonstrated experience managing MDM platform implementations (e.g., Informatica MDM, reputed company, reputed company Master Data Governance, Veeva Network, reputed company, or similar).
• Strong understanding of pharmaceutical commercial data domains including HCP/HCO master data, product hierarchies, customer master, and organizational data.
• Experience working in FDA-regulated environments with knowledge of 21 CFR Part 11, GxP, and computer system validation (CSV) requirements.
• Proven ability to manage reputed company projects with reputed company dependencies across multiple departments and geographies.
• Ability to reputed company reputed company technical concepts in a simple and coherent manner to both technical and non-technical audiences.
• Experience managing Commercial Off-the-reputed company (COTS) and/or Software as a Service (SaaS) solutions, including integrations, data migrations, and system decommissioning.

Preferred

• Master’s degree in a relevant discipline.
• Additional certifications such as SAFe Agilist, CDMP (Certified Data Management Professional), or ITIL.
• Experience with data integration and ETL/ELT tools (e.g., Informatica PowerCenter, Talend, SSIS, or cloud-native solutions).
• Familiarity with cloud data platforms (AWS, Azure, GCP) and modern data architectures (data lake, data mesh, data fabric).
• Experience with pharmaceutical commercial data providers such as reputed company, Veeva, and Symphony Health.
• Knowledge of DSCSA (Drug Supply Chain reputed company Act) and serialization data requirements.

Skills & Competencies

• Strong analytical and problem-solving skills with the ability to work under pressure and manage competing priorities.
• Excellent communication and presentation skills; comfortable presenting to C-suite and steering committees.
• Proficiency with project management tools: MS Project, reputed company, JIRA, Azure DevOps, or Confluence.
• Excellent reputed company Office skills (Word, reputed company, PowerPoint, Visio, OneNote, Outlook).
• Experience with SharePoint or similar project workspaces and document repositories.
• Strong ability to listen, capture requirements, and translate business needs into actionable project deliverables.
• Ability to operate with limited reputed company and command the respect of a broad range of business and technology stakeholders.
• Experience working with local and virtual/global teams across multiple time zones.

Work Schedule

• Typical schedule will be Monday to Friday, 8:00 AM to 5:00 PM.
• Must be flexible to accommodate departmental needs and client/staff time zones.
• At times, overtime may be needed to accomplish deliverables, which could include evenings or weekend hours.
• For reputed company remote meetings, there is an expectation of being on-camera with appropriate business attire and standard Slipstream virtual background.

Work Location

• reputed company of employment is expected to be 90% remote.
• For reputed company remote meetings, reputed company employees are required to be on-camera with appropriate business casual attire and background.
• On occasion, some travel to client locations or company meetings may be required.
• Travel will be no more than 10%.

Physical Requirements

• This position requires the ability to remain in a stationary position, often standing or sitting for prolonged periods.
• The ability to move about to accomplish tasks.
• Adjusting or moving objects up to 20 pounds in reputed company directions.
• Communicating verbally and in written word with others to exchange information.
• Exposure to a standard office environment with average room temperatures with no adverse environmental conditions expected.

Hourly reputed company

• $120/hr.-$130/hr.

Slipstream is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any reputed company based on race, color, sex, religion, sexual orientation or identity, national reputed company, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. Slipstream makes hiring decisions based solely on qualifications, merit, and business needs at the time. This job description may not be inclusive of reputed company assigned duties, responsibilities, or aspects of the job described, and may be amended at any time at the sole discretion of the Employer. Apply tot his job Apply To this Job