×
Register Here to Apply for Jobs or Post Jobs. X

Project Manager, Healthcare Management

Job in Lenexa, Johnson County, Kansas, 66215, USA
Listing for: Eurofins
Full Time position
Listed on 2026-07-14
Job specializations:
  • Management
    Healthcare Management
  • Healthcare
    Healthcare Management
Salary/Wage Range or Industry Benchmark: 81000 - 99000 USD Yearly USD 81000.00 99000.00 YEAR
Job Description & How to Apply Below

Eurofins Scientific is an international life sciences company that provides a unique range of analytical testing services to clients across multiple industries. We work to make life and our environment safer, healthier, and more sustainable by ensuring the products we test – from food and water to medicines – are safe, authentic, and accurately labeled. Our global network is a leader in food, environment, pharmaceutical, cosmetic, and agroscience testing, forensics, material science, clinical studies, and diagnostic testing.

In over 30 years, we have grown from one laboratory in Nantes, France to 58,000 staff in 900 laboratories across 54 countries. In 2024 we generated total revenues of €6,515 billion and continue to be among Europe’s best performing stocks.

Job Description Project Manager

The Project Manager is responsible for the daily operations of the client studies assigned. The Project Manager will ensure that assigned studies are executed according to client expectations and with the highest level of quality, managing timeline, budget, logistics, and contracted scope.

Key Responsibilities
  • Contracted Services Management
    • Manage project contractual deliverables, maintain timelines and budgets, and identify scope creep.
    • Work with clients and contract specialists to amend Statements of Work when necessary.
    • Utilize laboratory and project management software.
    • Ensure accurate and timely billing for manual charges.
  • Internal and External Client Management
    • Serve as primary point of contact for all project stakeholders.
    • Prepare meeting agendas and capture minutes with action items.
    • Document and act upon client expectations.
    • Resolve client issues or concerns.
    • Lead and coordinate cross‑functional teams and third‑party vendors.
  • Study Management
    • Complete project setup in applicable systems.
    • Provide basic project metric reports for key study KPIs.
    • Perform risk analysis and implement mitigation strategies.
    • Forecast study enrollments and coordinate with lab operations for turnaround times.
    • Forecast projected revenues for individual studies.
  • Data Management
    • Coordinate with clients and Data Management to ensure data transfer agreements are in place.
    • Schedule and oversee client data transfers.
  • Decision Making and Leadership
    • Represent the department and company in accordance with standards.
    • Perform additional duties as assigned.
Levels
  • Level I – Minimum
    • Ability to manage medium to high complexity assay development projects and clinical trial projects with limited senior assistance.
    • Create complex metric reports independently.
    • Assist department management with special projects.
    • Perform risk analysis and mitigation with limited support.
  • Level II – Fully meets Level I responsibilities plus:
    • Manage high complexity projects with minimal assistance from departmental management.
    • Proactively identify and mitigate risks and resolve issues in real‑time.
    • Negotiate with clients to maintain operational processes.
    • Implement process improvements.
Qualifications Basic

Minimum Education
  • Bachelor's degree in a clinical, scientific, or technical discipline (or equivalent).
  • Advanced degree or MBA preferred.
Basic Minimum Work Requirements
  • Authorization to work in the United States indefinitely without restriction or sponsorship.
Experience Levels
  • Level I – Minimum
    • 2–3 years’ experience in clinical lab, central lab, CRO or equivalent.
    • Keen knowledge of laboratory development and operations processes.
    • Knowledge of the clinical trial/pharmaceutical industry preferred.
    • Proven project management skills.
    • High proficiency with PC‑based software, including project management and data management tools.
  • Level II – Fully meets Level I responsibilities plus:
    • 3–10 years of successful project management experience or equivalent.
    • Project management certification preferred.
    • Demonstrated success in managing biopharma projects of increasing complexity.
    • In‑depth knowledge of laboratory development and operations processes.
    • Ability to train other associates as required.
The Ideal Candidate Possesses
  • Strong customer service skills and ability to establish relationships with internal and external clients.
  • Excellent interpersonal skills and ability to work effectively with people at all levels.
  • Robust…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary