Senior Clinical Supplies Specialist

hace 3 semanas

Ciudad de México, Ciudad de México Fortrea A tiempo completo
Job Title: Senior Clinical Supplies Specialist

Fortrea is seeking a highly skilled Senior Clinical Supplies Specialist to join our team. As a key member of our Clinical Supplies Services team, you will be responsible for coordinating and overseeing logistics related to clinical and ancillary supplies services.

Key Responsibilities:
  • Coordinate and oversee aspects of logistics related to Clinical and Ancillary Supplies services.
  • Support these services to both internal and external clients.
  • Responsible for the set-up and coordination of project activities related to clinical and ancillary supplies.
  • Independently support the delivery of the Clinical and Ancillary supplies component of assigned studies within a region or for a large global study.
  • Provide local support with clinical and ancillary 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 and ancillary supply 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 Covance requirements.
  • Provide logistical support for clinical and ancillary supply coordination.
  • Provide input into business development activities.
  • Act as a subject matter expert (SME) in client-focused clinical and ancillary supply workstreams.
Requirements:
  • 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.
  • 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 & 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%)
Preferred:
  • 2-4 years Clinical Supply Project Management logistics experience
  • Demonstrated Regulatory, GMP or QA experience.

Fortrea is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, sex, national origin, age, disability, or any other protected characteristic. We are committed to creating a diverse and inclusive workplace and encourage all qualified candidates to apply.

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