Senior Program Manager

Intellectt Inc; Maple Grove (MN); On-site; USD 62,000 - 69,000; Full time

Benefits offered by this job

Health Insurance

401(k) Plan

Paid Time Off (PTO) as per law

Job summary

Intellectt is seeking a Senior Program Manager, Clinical Data Review in Maple Grove, MN for a contract role. You will drive implementation of data review processes across Global Clinical Operations, leading cross-functional initiatives and coordinating stakeholders to ensure successful adaptation.

The ideal candidate has 8+ years in clinical research, strong program and change management skills, and excellent executive communication. Onsite work and fast-paced collaboration are 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 within a matrixed organization.
• Strong program management and change management skills.
• Excellent communication and executive presentation skills.
• Experience with clinical data review, reporting, and database-related processes.

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, risk assessments, dependencies, and communication strategies.
• Coordinate activities across clinical stakeholders and cross-functional teams.
• Drive stakeholder engagement, alignment, and collaboration.
• Support change management initiatives and process adoption.
• Facilitate governance meetings and prepare leadership updates.
• Monitor program progress, identify risks, and support issue resolution.
• Develop presentations and implementation materials for leadership.

Skills

Clinical Data Review

Stakeholder Influence

Program Leadership

Change Management

Executive Presentations

Cross-Functional Collaboration

Risk Management

Communication Skills

Education

Bachelor's degree in a scientific, healthcare, or related discipline

Job description

Job Title: Senior Program Manager, Clinical Data Review

Company: Intellectt

Location: Maple Grove, MN 55311

Employment Type: Contract

Duration: Not specified

Job Summary

The Senior Program Manager, Clinical Data Review will partner with Clinical Data Management leadership to drive the implementation and adoption of key data review processes across Global Clinical Operations. This role will lead business-critical initiatives through program planning, stakeholder coordination, change management, and execution across a complex, cross-functional environment. The ideal candidate will bring clinical trial experience, strong program leadership skills, and the ability to influence stakeholders and drive successful implementation.

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, risk assessments, dependencies, and communication strategies.
• Coordinate activities across clinical stakeholders and cross-functional teams.
• Drive stakeholder engagement, alignment, and collaboration.
• Support change management initiatives and process adoption.
• Facilitate governance meetings and prepare leadership updates.
• Monitor program progress, identify risks, and support issue resolution.
• 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 within a matrixed organization.
• Strong program management and change management skills.
• Excellent communication and executive presentation skills.
• Experience with clinical data review, reporting, and database-related processes.

Preferred Qualifications

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

Key Skills

• Clinical Data Review and Database Reporting
• Clinical Trial and Data Management
• Program and Project Leadership
• Stakeholder Management and Influence
• Change Management
• Executive Communication and Presentations
• Cross-Functional Collaboration
• Risk Management and Problem Solving
• Execution and Results Orientation

Work Requirements

• Must be available to work onsite in Maple Grove, MN, five days per week.
• Standard working hours are Monday through Friday, 9:00 AM–5:00 PM.
• Ability to coordinate with multiple teams and stakeholders in a fast-paced, global clinical operations environment.
• Expected to start as soon as possible after completing the required screenings.

Pay Range: $45-50/hr on W2

Benefits:

Employees hired into this position are eligible for the following benefits, subject to the applicable plan terms and eligibility requirements.

• Health Insurance: Medical, dental, and vision insurance options are available through a third-party provider. Employees are responsible for paying the full cost of their insurance premiums.
• Retirement Benefits: A 401(k) retirement savings plan is available. No employer matching or other employer contributions are provided.
• Paid Time Off (PTO): No PTO other than that required by applicable state and local laws

Equal Employment Opportunity (EEO)

Intellectt Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, disability, genetic information, veteran status, or any other characteristic protected by applicable federal, state, or local law.