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Project Management

Your dedicated Project Manager provides seamless communication while acting as your primary study contact. As a member of your team, our Project Manager will find solutions to facilitate your project objectives (scope, resources, time, budget, quality and satisfaction) from contract signature through project closure. To address questions and requests promptly, your Project Manager will liaise between both external and internal project teams. Your Project Manager takes the scope of work objectives for all phases of the trial to join them with systematic efficiencies to contribute to the success of your project.

Ensures Your Laboratory Service Requirements are Planned, Communicated, and Expertly Executed

  • Capable of rapid study set-up to fulfill critical timelines
  • >250 studies performed in the last three years spanning Phase I through Phase IV testing supported by project management with global clinical trial experience
  • Adherence to contracted budgets and turnaround times*
  • Collaboration with sponsor, CRO, clinical sites and others at direction of sponsor
  • Kit production and supply management - study specific kits and investigator manuals

*Turnaround times listed within the test menu of this website are applicable to clinical samples only (e.g. patient samples from hospitals or reference laboratories). To discuss BioPharma/clinical trial testing turnaround time needs, please contact

Information Technology

In cooperation with your Project Manager, a dedicated project Data Coordinator can provide a number of services to help accelerate and simplify your secure data transfer and laboratory reporting needs. Each study is unique, and we want to ensure your data is received in a format that complies with your specific needs. We support standard electronic data transfer formats (EXCEL, CSV, ZIP) in addition to non-standard data transfer formats (SAS, CDISC).

Commitment to Quality

Viracor Eurofins is committed to providing the highest quality service to its clients in compliance with all federal, state, and local laws and regulations, as well as, organizational policies and ethical standards. Regulatory compliance is essential in successfully bringing diagnostic testing platforms and new therapeutic agents to the marketplace


Rely on innovative, specialized testing. Our R&D scientists partner with you to design, optimize, transfer and validate customized assays based on the specific needs of your protocol.  Our high-throughput clinical laboratory can support your clinical trials with fast turnaround times, large sample volumes and seamless validation and transfer.


Depend on diligence and agility. With short study set up timelines and rapid testing turnaround times, our Project Managers and Scientists act as an extension of your team – going above and beyond to get you results.


Trust in an experienced laboratory.  Your study deserves a lab that has over 30 years of specialized experience in molecular infectious disease testing, immune response monitoring, vaccine safety/efficacy assessment and allergy/hypersensitivity testing.

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