AGILE PROGRAM MANAGER
3B Staffing LLC
Job Title: Program Manager - Pharmaceutical / Life Sciences
Location: Waukegan, IL (Onsite)
Employment Type: Contract
GC/USC
About the Role:
Program Manager to lead and oversee strategic initiatives within the pharmaceutical and life sciences domain. This onsite role is ideal for a proven leader who excels at managing complex, multi-stream programs in regulated environments .
7+ years in pharma/biotech/CRO program management, experience leading multi-stream initiatives in regulated environments, strong GxP/compliance knowledge, proficiency in MS Project/Smartsheet/Jira, and excellent communication and stakeholder management skills.
Key Responsibilities:
Location: Waukegan, IL (Onsite)
Employment Type: Contract
GC/USC
About the Role:
Program Manager to lead and oversee strategic initiatives within the pharmaceutical and life sciences domain. This onsite role is ideal for a proven leader who excels at managing complex, multi-stream programs in regulated environments .
7+ years in pharma/biotech/CRO program management, experience leading multi-stream initiatives in regulated environments, strong GxP/compliance knowledge, proficiency in MS Project/Smartsheet/Jira, and excellent communication and stakeholder management skills.
Key Responsibilities:
- Lead large-scale, multi-stream programs within pharma, biotech, or CRO settings.
- Ensure compliance with GxP workflows, documentation systems, and regulatory standards.
- Collaborate with cross-functional teams to drive project execution and operational excellence.
- Track program progress, risks, and deliverables using tools such as MS Project, Smartsheet, Jira, or equivalents.
- Manage stakeholders effectively, providing updates, influencing decisions, and ensuring alignment with organizational goals.
- Facilitate process improvements, program governance, and adherence to compliance protocols.
- 7+ years of program or project leadership experience in pharma, biotech, or CRO environments .
- Proven success managing large, multi-stream initiatives in regulated settings.
- Strong understanding of GxP workflows , documentation systems, and compliance requirements.
- Proficiency in MS Project, Smartsheet, Jira , or equivalent project management tools.
- Excellent communication, leadership, and stakeholder management skills .
- Hands-on experience with VEEVA Vault (Clinical, Quality, or Regulatory modules).
- PMP, PgMP, or equivalent certifications .
- Familiarity with Agile, hybrid, or scaled delivery methodologies .
Vacancy posted 3 days ago
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