Covance by Labcorp Job - 37906421 | CareerArc
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Company: Covance by Labcorp
Location: Bannockburn, IL
Career Level: Associate
Industries: Healthcare, Pharmaceutical, Biotech


Job Overview:

Whether it's at home, school, the office or other alternate location, GlobalCare's ambulant care services for clinical trials conveniently bring visits to the study patient. GlobalCare maintains a global network of multi-lingual Country Coordinators and local traveling service providers (nurses and physicians).


We are seeking a Clinical and Ancillary Supply Services Specialist to join our team in Bannockburn, Illinois.




Serve as primary liaison between Clinical & Ancillary Supply Services, operational project teams, Covance Laboratory Services (CLS), distribution vendors, client distribution units, packaging and labeling vendors


  • Liaison with project teams and department members regarding issues of compliance with ICH/GCP, GMP, project plans, and Covance SOPs.
  • Oversee coordination of study related Clinical and Ancillary Supply activation and maintenance components including Labels/Supply, Import/ Export requirements, ancillary supply management.
  • Develop project specific plans for the Clinical and Ancillary supply component of assigned studies.
  • Represent Clinical and Ancillary supplies component within a region or for complex global studies at client and internal project meetings.
  • Anticipate and monitor project requirements and institute appropriate actions to ensure timelines and budget needs are met.
  • Contribute to the development of processes, procedures, tracking systems and IT solutions for Clinical and ancillary supply activities.
  • Interact with internal and external work groups to evaluate and forecast workload and resource needs.
  • Ensure appropriate communication on project-related matters with the clinical project team.
  • Provide consultation pertaining to clinical & ancillary supplies: the labeling, tracking, specific national requirements, importation, etc.
  • Bachelor's degree in a life science is strongly preferred


  • Minimum of 4 years relevant clinical research experience in a pharmaceutical company/CRO,
    including at least 2 years of clinical and ancillary supplies management responsibility
  • Very strong technical writing skills and analytical skills
  • Strong networking abilities and an ability/willingness to work with individuals across the globe
  • Excellent communication, planning, and organizational skills
  • Experience in end to end (full service) clinical trial management, ideally with global project
    management experience
  • Abilities to review/analyze relevant data so as to build evidence-based clinical trial strategies
  • Abilities to design/develop effective strategies to bring about trial success, as defined by clients
    and project teams through the use of an evidence-based approach
  • Strong computer skills with an ability to understand and access and leverage technology
  • Ability to work independently


  • 2-4 years Clinical Supply Project Management logistics experience
  • Demonstrated Regulatory, GMP or QA experience

 Apply on company website