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Sr. Program Manager – Clinical Data Review

Generis TEK Inc.Maple Grove, MN🇺🇸United States

Quick overview

Salary$55/hr
SeniorityMid Senior
Work modeOn Site
LocationMaple Grove, MN, United States
Stakeholder ManagementPMP

Job description

Please Contact: To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Michelle Singh at email address can be reached on # .
We have Contract role Sr. Program Manager – Clinical Data Review for client at Maple Grove, MN. Please let me know if you or any of your friends would be interested in this position.
Position Details:
Sr. Program Manager – Clinical Data Review- Maple Grove, MN
Location                       : 6820 Wedgewood Road N., Maple Grove, MN – 55311 (100% Onsite)
Project Duration      : 6 Months of contract
Shift Timing               : 9:00 AM to 5:00 PM (Mon to Fri)
Pay Rate                      : $55.00 per hour on W2
Position Summary:
The Senior Program Manager, Data Review partners with Clinical Data Management leadership to drive the implementation and adoption of key Data Review processes across Global Clinical Operations. This role will support multiple business-critical initiatives by providing program leadership, stakeholder coordination, change management, and execution support across a complex cross-functional environment. The successful candidate will combine clinical trial experience, strong program management skills, and the ability to influence stakeholders to ensure initiatives are delivered effectively and adopted across the organization.
Key Responsibilities:

  • Partner with the Principal Clinical Data Manager and cross-functional stakeholders to implement new Data Review processes and capabilities.
  • Develop and maintain program plans, timelines, risks, dependencies, and communication strategies.
  • Coordinate activities across key clinical stakeholders.
  • Drive stakeholder engagement and alignment.
  • Support change management and adoption activities.
  • Facilitate governance meetings and leadership updates.
  • Monitor program progress and risks.
  • Develop presentations and implementation materials for leadership.


Required Qualifications:

  • Bachelor's degree in a scientific, healthcare, or related discipline.
  • 8+ years of clinical research experience.
  • Experience leading cross-functional programs or process implementations.
  • Strong understanding of clinical trial execution and clinical data management.
  • Ability to influence stakeholders in a matrixed organization.
  • Strong program management and change management skills.
  • Excellent communication and executive presentation skills.


Preferred Qualifications:

  • Medical device clinical trial experience.
  • Experience with clinical data review processes.
  • Experience supporting global organizations.
  • PMP, Prosci, or similar certification.
  • Advanced degree (MS, MBA, MPH, or equivalent).


Top Skills:

  • Clinical Data Base Reporting
  • Experienced Program/Project Leadership
  • Ability to jump in and work at a high level with multiple teams/stakeholders


Critical Competencies:

  • Clinical Trial & Data Management Knowledge
  • Program & Project Leadership
  • Stakeholder Influence
  • Change Management
  • Executive Communication
  • Cross-Functional Collaboration
  • Problem Solving & Decision Making
  • Execution & Results Orientation


To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Michelle Singh at email address can be reached on # .

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