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Sr. Program Manager

The Fountain Group LLC

Maple Grove, MN 55311 • 10/28/2026

Job Description

Job Description

The Fountain Group iscurrently seeking a Sr. Program Manager – Clinical Data Reviewfor a prominent client of ours. This position is located at Maple Grove, MN.Details for the position are as follows:

Sr. Program Manager – Clinical Data Review
Location: 6820 Wedgewood Road N., Maple Grove, MN (100% Onsite)
Pay Rate: $53–$57/hr
Duration: 6-Month Contract (Extension Potential)
Schedule: Monday–Friday, Daytime Hours

Job Description

Seeking a Senior Program Manager to lead the implementation and adoption of clinical data review processes across Global Clinical Operations. This role partners with Clinical Data Management leadership and cross-functional stakeholders to drive clinical process improvements, program execution, and organizational change.

  • Lead implementation of clinical data review processes and capabilities across clinical operations.

  • Develop and manage program plans, timelines, milestones, risks, dependencies, and deliverables.

  • Coordinate cross-functional clinical stakeholders and drive alignment on program objectives.

  • Support change management, process implementation, and organizational adoption.

  • Facilitate governance meetings and prepare executive presentations, implementation materials, and leadership updates.

  • Monitor program progress, identify risks, and drive timely execution of key initiatives.

Education
  • Bachelor’s degree in a scientific, healthcare, or related discipline.

  • Advanced degree (MS, MBA, MPH, or equivalent) preferred.

Required Skills
  • 8+ years of clinical research experience.

  • Strong clinical data management knowledge, including clinical trial data review and database reporting.

  • Program and project leadership experience in clinical research or clinical operations.

  • Experience leading cross-functional programs and process implementations.

  • Clinical trial execution and clinical data review process knowledge.

  • Program planning, timeline management, risk tracking, and dependency management.

  • Stakeholder management, change management, and implementation support.

  • Executive presentations and program status reporting.

Preferred Skills
  • Medical device or pharmaceutical clinical trial experience.

  • Experience implementing clinical data review processes across global organizations.

  • PMP, Prosci, or equivalent project management or change management certification.

  • Advanced experience partnering with Clinical Data Management leadership.

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