• Logistics Deployment Coordinator

    Job Locations US-PA-Plymouth Meeting, PA. USA
    Job ID
    Position Type
    Permanent Employee - Full-Time
  • Role Overview

    Logistics Deployment Coordinator - Plymouth Meeting, PA


    The Logistics deployment coordinator supports the Customer Delivery teams to make sure that client deliverables are shipped on time. 


    Key Accountabilities/Decision Making & Influence

    • Handles daily project logistics correspondence between Logistics and the Project Teams
    • Attend internal project kick off meetings.
    • Attend client calls as requested
    • Work with the Procurement team and the Inventory team to make sure study supplies are ordered / allocated and organize equipment to be in the relevant warehouses prior to study go live
    • Generate Commercial invoice documentation for shipping tickets
    • Maintain device certification library including new products that are added to CRF Health Portfolio
    • Negotiate shipping schedule with the logistics shipping team
    • Create Shipping tasks in NetSuite
    • Maintain device / country requirement export database
    • Track all shipments to delivery and communicate any delays to the project team
    • Maintain shipping forecast/schedule

    Knowledge, Skills & Attributes

    • A background working in a logistics role, ideally for at least 2 years.
    • Minimum education:  High School graduation 
    • Understanding and/or experience of clinical trials / pharmaceutical industry is an advantage.
    • Must have excellent time management, communications, and organizational skills.
    • Customer Service experience preferred
    • Must be able to communicate effectively with the project teams
    • Able to multi-task and work with multiple team members. 
    • Must be a team oriented person with a “can do” attitude.


    About CRF Health

    Global Leader in eCOA Solutions for Clinical Trials 


    CRF Health is a global leader in eCOA (electronic Clinical Outcome Assessments) solutions for the life sciences industry. eCOA encompasses PROs (Patient Reported Outcomes), ObsROs (Observer Reported Outcomes) and ClinROs (Clinician or Rater Reported Outcomes) with outstanding project management focused on delivering value for our customers.  Committed to driving the change to higher quality outcomes and more efficient paper-free clinical trials through improved patient engagement, our intuitive and patient-focused eCOA technology helps companies bring new medicines to market quickly, safely and more cost-effectively. Our complete eCOA solutions are ideal for home and site-based phase I-IV clinical trials across the world for many therapeutic areas and patient populations.  More information to be found on our website.  





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