Project Manager II

IT Engagements; Arizona; On-site; USD 90,000 - 120,000; Full time

Job summary

IT Engagements in the United States seeks an experienced Project Manager II - CDx Pharma Services to lead cross-functional initiatives from concept to completion in Tucson, AZ. You will develop detailed work plans, manage schedules, resource planning, and status reports while ensuring compliance and timely delivery in a fast-paced life sciences environment.

Ideal candidates have 2–5 years in project management within diagnostic/pharma/biotech, strong communication, and proficiency with MS

Qualifications

• Bachelor's degree; Life sciences preferred.
• 2–5 years of PM experience in diagnostic, medical device, pharma, or biotech.
• Strong communication and organization skills.
• Ability to lead diverse, cross-functional teams.
• Proficiency with MS Office and project management tools.

Responsibilities

• Project Execution & Improvement: Manage multiple projects from initiation through completion.
• Operations & Compliance: Ensure deadlines and compliance with the service plan.
• Resource & Data Management: Maintain data integrity of resource trackers and dashboards.
• Strategic Best Practices: Drive continuous improvement and knowledge exchange.
• Risk & Requirement Management: Identify risks and perform critical path analysis.
• Stakeholder Management: Engage and align diverse stakeholders on goals.

Skills

Communication

Organization

Cross-functional leadership

Stakeholder management

Problem solving

Education

Bachelor's degree (Life sciences preferred)

Tools

MS Office

MS Project

Google Workspace

Job description

Greetings from IT Engagementss

IT Engagements is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. We have an immediate opening for the below position with one of our premium clients.

Job Title: Project Manager II - CDx Pharma Services

Location: Tucson, AZ

As a Project Manager II - CDx Pharma Services, you will play a key role in optimized product delivery and be accountable for all project management aspects of projects ranging from simple to complex. You will drive projects and products from the original concept through completion by developing and directing detailed work plans, schedules, project estimates, resource planning, and status reports.

We are looking for a highly autonomous self-starter who exercises independent judgment, proactively resolves challenges, and excels with minimal supervision. The ideal candidate is a motivated self-learner and go-getter who takes the initiative to learn, drive projects to completion, and thrive in dynamic environments. As a trusted advisor, you will translate project needs into tangible outcomes, enabling the organization to use energy and time effectively while quickly responding to changing business needs.

KEY RESPONSIBILITIES

• Project Execution & Improvement: Manage multiple small and large improvement projects, process improvement projects, and other business-related initiatives from initiation through completion. Track progress of activities and manage execution of cross-functional plans.
• Operations & Compliance: Facilitate cross-functional interactions to ensure projects are completed within deadlines and in compliance with the service plan. Oversee and guide day-to-day activities of sample process flow and accurate reporting of results.
• Resource & Data Management: Responsible for the data integrity of resource trackers and capacity charts, ensuring projects align with best practices. Manage the CAPEX budget, update/maintain dashboards, and communicate project reports to stakeholders.
• Strategic Best Practices: Implement and pull in best practices within the clinical sciences team; foster continuous improvement by ensuring knowledge and experience exchange.
• Risk & Requirement Management: Proactively identify project risks, potential bottlenecks, or delays; challenge assumptions, and perform critical path analysis. Maintain clear documentation of project requirements and conduct "lessons learned" sessions to drive future improvement.
• Stakeholder Management: Engage, influence, and manage a diverse group of stakeholders, ensuring all partners are aligned on project goals and deliverables.

TOP SKILLS, EXPERIENCE, AND EDUCATION

Required Qualifications

• Education: Bachelor's degree (Life sciences preferred)
• Experience: 2-5 years of experience in project management within the diagnostic, medical device, pharmaceutical, or biotech industry, leading product development or process improvement projects.
• Soft Skills & Attributes:
  • Exceptional communication and organization skills.
  • Proven ability to work through unknowns and ambiguity with a solution-oriented mindset.
  • Demonstrated capability in managing diverse, cross-functional stakeholders.
• Technical Proficiency:
  • Advanced proficiency in MS Office (Word, Excel, PowerPoint), including MS Project.
  • Proficiency in the Google Suite environment
• Speed & Agility:
  • Experience with projects or business initiatives that require rapid activity achievement.

Preferred Qualifications

• Advanced Education: Master's degree
• Certification: PMP (Project Management Professional) certification
• Methodology Experience: Experience with Scrum/Agile project management methodologies