Job Overview:
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 and 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 Fortrea 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.
Summary of Responsibilities:
Understand and follow, provide input to and training of related project specific and Fortrea policies and procedures.
Direct line management responsibility for Clinical and Ancillary Supply Services team members; the recruitment, training/development, allocation, supervision, utilization, and performance review of assigned personnel.
Effectively network with others throughout Fortrea.
Serve as primary liaison between Clinical and Ancillary Supply Services, operational project teams, Fortrea Laboratory Services (CLS), distribution vendors, client distribution units, packaging and labeling vendors or assign relevant staff to carry out this function.
Liaison with project teams and department members regarding issues of compliance with ICH/GCP, GMP, project plans, and Fortrea 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.
Assist in the preparation and presentation of services, costings, and proposals for new business.
Management of relevant portion of project budgets, including input into preparation of utilization reports (projected and vigente) and implement measures to ensure accurate billing.
Interact with internal and external work groups to evaluate and forecast workload and resource needs.
Present at internal and external meetings including client meetings.
Ensure appropriate communication on project-related matters with the clinical project team.
Provide clinical and ancillary supply project related milestone information.
Review and, in accordance with Fortrea standards and assigned authority, approve employee expense reimbursement.
Clinical trial supply and ancillary supply coordination:
Provide consultation pertaining to clinical and ancillary supplies: the labeling, tracking, specific national requirements, importation.
Review IxRS specifications.
Ensure triggering of drug shipments to investigational sites.
Manage Drug distributor.
Supervise development and review of Clinical Trial Supplies Plans.
Review of and input to authority inspection and client audit findings or CAIRs.
Develop, update and/or refine SOPs.
Remain current with and provide updates to regional and local regulatory requirements related to clinical and ancillary supplies.
Remain current with industry innovations and advances, especially pertaining to clinical and ancillary supply matters so as to include relevant advances and technology into the design of trial strategies.
Maintain relationships with comparable levels at client organizations to ensure effective relationships.
Build and develop relationships with new clients to bring in new business.
Serve as an escalation point for project issues.
Involvement in strategic partnership discussions.
Input into client projects.
All other duties as needed or assigned.
Qualifications (Minimum Required):
University/College Degree (preferably postgraduate degree) AND 4 years relevant clinical research/GMP experience.




Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Thorough understanding of global drug development and the clinical trial project management process, with a special emphasis on investigator sites, patient recruitment and retention.
Thorough and practical working knowledge of ICH-GCP Guidelines, Clinical GMP, including relevant international requirements/guidelines for the conduct of global clinical development programs.
In lieu of the above requirements, candidates with greater than six (6) years clinical research experience including monitoring in the pharmaceutical or CRO industries will be considered.
Language Skills Required:
Speaking/Writing/Reading: English + local language.
Experience (Minimum Required):
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.
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.
Preferred Qualifications Include:
3 years' Experience in Clinical Supply distribution/ GMP environment.
An understanding of aspects surrounding Fortrea business development (time and cost estimates, bid defense, contracts).
An understanding of Fortrea procedures, including Standard Operating Procedures.
2-4 years Clinical Supply Project Management logistics experience.
Demonstrated Regulatory, GMP or QA experience.
Physical Demands/Work Environment:
General Office Environment.
Travel Requirements:
International and Domestic travel may be required *****% of the time, including air travel and overnight stays.
Ability to drive and possess a valid driver's license.
Ability and willingness to present at internal and external meetings.
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📌 Logistics Manager (Buenos Aires)
🏢 Fortrea
📍 Buenos Aires