Clinical Supply Chain Manager

hace 6 días


Ciudad de México, Ciudad de México Fortrea A tiempo completo

At Fortrea, we are seeking an experienced Clinical Supply Chain Manager to join our team. The salary for this role is approximately $90,000 per year, based on industry standards and location.

About the Role

This is a Senior Specialist position responsible for coordinating and overseeing logistics related to clinical supplies services. The successful candidate will support these services to both internal and external clients, set up and coordinate project activities related to clinical supplies, and independently support the delivery of clinical supplies components of assigned studies.

Key Responsibilities
  • Coordinate and oversee aspects of logistics related to clinical supplies services.
  • Support these services to both internal and external clients.
  • Responsible for the set-up and coordination of project activities related to clinical supplies.
  • Independently support the delivery of the clinical supplies component of assigned studies within a region or for a large global study.
  • Provide local support with clinical supplies start-up activities and related project feasibility.
  • Act as a subject matter expert (SME) related to import, export, and labeling requirements.
  • Work with staff in Clinical Trial Design & Strategy, Vendor Management, Quality Assurance, Business Development, and Operations to provide relevant clinical supplies data critical to the ability of the organization to develop plans for the successful implementation and conduct of global clinical trials.
  • Assure that pre-study, drug supply, and labeling processes comply with applicable guidelines and regulations and fulfill client and Fortrea requirements.
  • Provide logistical support for clinical supplies coordination.
Requirements

To be considered for this role, you must have:

  • A minimum of 4 years relevant clinical research experience in a pharmaceutical company/CRO, including at least 2 years of clinical supplies management responsibility.
  • University/College Degree (preferably postgraduate degree)
  • Fluent English
  • 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
  • Ability to inspire, to lead by example, and motivate teams to seek solutions and get results
  • Strong abilities to negotiate and liaise with customers in a professional manner
  • 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 alternatives.
  • Ability to work independently
  • Availability to travel (10-20%)


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