Sr. Project Manager

Posted 3 Hours Ago
Be an Early Applicant
Hiring Remotely in Baltimore, MD, USA
In-Office or Remote
125K-135K Annually
Senior level
Healthtech • Biotech
The Role
Leads large, complex, cross-functional projects from initiation through delivery, managing scope, schedules, budgets, risks, documentation, governance, and stakeholder communications. Partners with program and functional leaders to align projects with strategic priorities, mentors project managers, and improves project management practices. The role supports regulated life sciences product and software development across multiple lifecycle stages, including FDA-regulated initiatives.
Summary Generated by Built In

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.


Labcorp Oncology is seeking a Sr. Project Manager to join our team.

Work Schedule: Monday - Friday, 1st Shift

Job Summary:

The Sr. Project Manager is a strategic leader responsible for driving the successful delivery of large, complex, and cross-functional projects across diverse technologies and business domains. This role requires exceptional leadership and the ability to navigate ambiguity, align stakeholders, and maintain momentum in dynamic environments. Sr. Project Managers are accountable for delivering outcomes on time, within scope, and on budget, managing multiple initiatives simultaneously. They excel at identifying and mitigating risks, communicating project health and success probability across all organizational levels, and seeing the big picture to ensure alignment with broader business goals. With deep expertise in project management fundamentals, they serve as mentors and change agents, continuously improving delivery practices and enabling organizational growth.

Job Responsibilities:

  • Lead the end-to-end delivery of large-scale, strategic projects with high complexity, cross-functional impact, and visibility across the organization.
  • Develop and maintain detailed project plans, including task dependencies, milestones, deliverables, and resource allocations, ensuring alignment with business objectives.
  • Collaborate closely with Program Managers to ensure project alignment within broader program goals, portfolio priorities, and strategic initiatives.
  • Proactively identify, assess, and prioritize risks; develop and implement robust mitigation strategies to minimize impact and ensure project continuity.
  • Navigate ambiguity and evolving requirements by applying sound judgment, adaptability, and strategic foresight to keep projects on track.
  • Partner with department leads, product managers, and functional stakeholders to resolve major challenges and ensure successful project outcomes.
  • Provide clear, concise, and actionable project updates to senior leadership, influencing strategic decisions and organizational direction.
  • Monitor and manage project performance against scope, schedule, and budget; escalate issues appropriately and drive resolution through effective governance.
  • Oversee project financials, including budget planning, expense tracking, and variance analysis to ensure fiscal accountability.
  • Ensure project documentation is complete, accurate, and accessible; address gaps in ownership or accountability to maintain momentum.
  • Foster cross-functional collaboration to overcome obstacles and drive projects toward successful delivery.
  • Mentor and guide other project managers, sharing best practices, tools, and techniques to elevate project management maturity across the organization.
  • Contribute to continuous improvement of project management processes, tools, and methodologies at both the project and portfolio level.
  • Champion a culture of transparency, accountability, and results-driven execution across project teams.

Minimum Qualifications:

  • 5 or more years of project management experience
  • 3 or more years of experience within biotech, molecular diagnostics, medical device, or a similarly regulated life sciences industry
  • 3 or more years of experience leading complex, cross-functional product and software development projects,
  • 3 or more years of experience managing projects across multiple stages of the product development lifecycle.

Preferred Qualifications:

  • Bachelor’s degree in project management, scientific, engineering, business, or related discipline
  • PMP certification
  • 2 or more years of experience supporting or leading FDA-regulated product development

Additional Job Standards:

  • Familiarity with 510(k), PMA, or comparable regulatory pathways
  • Ability to partner with program, portfolio, and functional leadership to support project prioritization, resource planning, risk management, and decision-making.

Application Window: 8/19/26 - 8/22/26

Pay Range: $125k - $135K

All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. 

Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. For more detailed information, please click here. 


Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. 


We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.


Skills Required

  • 5 or more years of project management experience
  • 3 or more years of experience within biotech, molecular diagnostics, medical device, or a similarly regulated life sciences industry
  • 3 or more years of experience leading complex, cross-functional product and software development projects
  • 3 or more years of experience managing projects across multiple stages of the product development lifecycle
  • Bachelor's degree in project management, scientific, engineering, business, or related discipline
  • PMP certification
  • 2 or more years of experience supporting or leading FDA-regulated product development
  • Familiarity with 510(k), PMA, or comparable regulatory pathways
  • Ability to partner with program, portfolio, and functional leadership to support project prioritization, resource planning, risk management, and decision-making
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The Company
HQ: Burlington, NC
19,796 Employees
Year Founded: 1978

What We Do

We believe in harnessing science for human good. And so we work day and night, around the world, to deliver answers for all your health questions—whether you’re a provider, drug developer, hospital, medical researcher or patient. That means everything from advancing diagnostic testing to helping launch new drugs, to offering new perspectives through data - all drawing from a deep well of scientific expertise. So when you need trusted information to make clear, confident health decisions, consider us your source.

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