Project Manager

ZP Group

United States

Remote

USD 83,000 - 110,000

Full time

14 days+
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Benefits offered by this job

Medical benefits
Dental benefits
Vision benefits
401(k)
PTO
6-month contract

Job summary

Piper Companies in the United States is seeking a Project Manager to support a leading life sciences and clinical research organization. The Project Manager will lead regulatory technology and business transformation initiatives, bridging business stakeholders and technical teams to ensure timely delivery of regulatory systems and process improvements.

Responsibilities include end-to-end planning, risk management, and coordinating with Regulatory Information Management, Publishing, and IT.

Qualifications

  • 8+ years of project management experience in regulated life sciences environments.
  • Regulatory affairs experience with RIM and publishing processes.
  • Hands-on experience leading Veeva implementations or related system deployments.
  • Ability to translate requirements across stakeholder groups and lead cross-functional teams.

Responsibilities

  • Lead end-to-end planning, execution, governance, and delivery of multiple program initiatives.
  • Manage project plans, milestones, risks, issues, dependencies, and executive communications.
  • Serve as the connection point between Regulatory Information Management, Publishing, business operations, and technical teams.
  • Support implementation activities involving Veeva platforms and regulatory content management solutions.
  • Facilitate decision-making, change management, and knowledge transfer activities.
  • Ensure objectives, regulatory requirements, and technical deliverables stay aligned.

Skills

PM leadership
Regulatory Affairs
Veeva implementations
Cross-functional collaboration
Governance & risk management

Tools

Veeva Vault

Job description

Piper Companies is seeking a Project Manager to support a leading organization within the life sciences and clinical research industries. The Project Manager will lead multiple regulatory technology and business transformation initiatives, serving as the bridge between business stakeholders and technical teams, working to ensure successful delivery of regulatory systems and process improvements.

Responsibilities of the Project Manager:
  • Lead end-to-end planning, execution, governance, and delivery of multiple program initiatives.
  • Manage project plans, milestones, risks, issues, dependencies, and executive-level communications across complex workstreams.
  • Serve as the connection point between Regulatory Information Management (RIM), Publishing, business operations, and technical teams.
  • Support implementation activities involving Veeva platforms, regulatory content management solutions, and system integrations.
  • Facilitate stakeholder decision-making, escalation management, organizational change management, and knowledge transfer activities.
  • Ensure business objectives, regulatory requirements, and technical deliverables remain aligned throughout the project lifecycle.
Qualifications of the Project Manager:
  • 8+ years of project management experience within life sciences, pharmaceutical, biotechnology, medical device, or other regulated environments.
  • Regulatory Affairs experience with a strong understanding of RIM, Publishing, and related regulatory operations processes.
  • Hands-on experience leading Veeva implementations, enterprise system deployments, or business transformation initiatives.
  • Strong ability to translate requirements across stakeholder groups.
  • Proven ability to provide direction and lead cross-functional teams through complex projects and organizational change.
  • Excellent communication, governance, risk management, and stakeholder management skills.
Compensation for the Project Manager includes:
  • Pay Range: $60-$80 per hour (depending on experience),
  • Comprehensive benefits package including medical, dental, vision, 401(k), and PTO
  • 6 Month Contract

This job opens for applications on 09/21/2026. Applications for this job will be accepted for at least 30 days from the posting date.

SEO Keywords

Project Manager, Regulatory Affairs, Global Regulatory Data and Information Systems, GRID Program, GRIDS Program, Regulatory Information Management, RIM, Regulatory Publishing, Veeva, Veeva Vault, Regulatory Operations, Life Sciences Project Manager, Medical Device Regulatory, Pharmaceutical Technology, Business Transformation, Digital Transformation, System Implementation, Technology Implementation, Cross-Functional Leadership, Program Governance, Change Management, Stakeholder Management, Regulatory Systems, Enterprise Project Management, Regulatory Content Management

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