Global Project Manager – Personalized Healthcare
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Description
Our client, a world leader in biotechnology and life sciences, is looking for a “Global Project Manager – Personalized Healthcare” based in Tucson, AZ(Hybrid).
Job Duration: Long Term Contract (Possibility of Extension)
Pay Rate: $62/hr on W2
Company Benefits: Medical, Paid Sick leave(as per state policy)
Seeking an experienced Project Manager with a biotech/pharmaceutical or diagnostics background to lead Companion Diagnostics (CDx) product development projects from concept through launch. The role involves managing project timelines, budgets, resources, risks, and scope while coordinating cross-functional teams and external pharmaceutical partners.
Key Responsibilities
- Lead CDx development projects and manage deliverables from initiation through launch.
- Develop and maintain project schedules, critical paths, budgets, resource plans, and status reports.
- Manage project scope, change requests, risks, dependencies, and mitigation plans.
- Coordinate internal stakeholders, cross-functional teams, and external pharmaceutical partners.
- Track contract milestones, project expenditures, FTEs, and invoice forecasts.
- Ensure compliance with quality management systems and applicable regulatory requirements.
- Apply project management methodologies, including hybrid Agile/Waterfall and SAFe practices.
Required Qualifications
- Bachelor’s degree, preferably in Life Sciences or a related field.
- 4+ years of project management experience in biotech, pharmaceuticals, diagnostics, or medical devices, leading product development projects.
- At least 1 year of experience in CDx, IVD, clinical biomarker development, analytical/clinical validation, regulatory submissions, or instrument/systems development.
- Experience working in a regulated industry, such as FDA-regulated or ISO-certified environments.
- Proficiency with Planisware, MS Office, Google Suite, and project management tools.
- Working knowledge of Agile, SAFe, and hybrid Waterfall-Agile methodologies.
Preferred Qualifications
- Master’s degree with 6+ years of relevant industry experience, or PhD with 3+ years of project management experience.
- Experience managing complex projects with external pharmaceutical partners.
- PMP and/or SAFe certification.
If interested, please send us your updated resume at
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