Manuel Longfellow Martinez Q. Email & Phone Number

Ciudad De México, México

Ciudad De México, México

México

- Responsible to manage the Clinical Trial Distribution protocols as well as the Direct to – Patient Programs.- Ownership for the clinical trial project, primary contact point, and act as “project owner” to coordinate the internal projects.- Responsible for managing the overall set-up of the trial creating work instructions, building protocols in the.

Ciudad De México Y Alrededores, México

• Manage WH & D of multiclient. (Pharma, Automotive, High Tech, chemical industry and Medical Device)
• Responsible of the revenue ($350,000 USD Monthly)
• Responsible of the P&L, Forecast & Budget.
• Ensure the implementation of the continuous improvement projects for savings and cost reduction (LEAN CULTURE)
• Create policies and procedures for new repository system (PolicyTech.com)
• Create the layout for the new warehouse in Merck.

México

• Responsible for Customer Service the Regional Strategy for complete Order to Cash process was developed, considering systems, head counts, procedures, and other resources for a correct spin off implementation, without.
• Freight and warehouse costs monitoring. Main focus to ensure adherence to logistics and distribution cost budgets. Strong monitoring and deviation analysis resulted in transportation costs and packaging material costs.
• Responsible of placing internal purchase orders of finished goods into the ERP, and do follow up activities until delivery to warehouse/customer. Improved shipment planning by reducing number of shipments during the.
• Responsible for finished goods inventory levels monitoring. Main focus on provide recommendations for a better inventory handling and control. Currently inventory levels controlled are in compliance with company’s.

Mexico

- Generate new business, develop and grow existing accounts by identifying and closing business opportunities. I have got the planning of the laboratory kits from AMGEN, I contacted 3 laboratories in order to offer our services.- Lead the logistic team during the projects Life cycle linked with AMGEN, ALCON and Pfizer. - Key contribution in the development.

Ciudad De México Y Alrededores, México

- Delivering Global Strategies for Process Development into Clinical Trial Supply Area.- Responsible For Investigational Product Labeling Process Ensuring the Adherence to Regulatory Guidelines at Mexico, Brazil, India, UK- Oversees the logistics aspects of designated projects to ensure that the right supplies are delivered to the right locations at the.

Mexico City

• Deliver Global Strategies for Process into the Clinical Supply Area.
• Responsible for Product Labeling process ensuring the adherence to regulatory guidelines in Mexico.
• Establish a closer interaction and clear communication channel with all partners Foreign Trade, Marketing, Sales Finance, Legal area, Drug Regulatory Affairs, Quality Assurance.
• Provide support for development of projects specific logistic strategy, execute clinical logistics procedures.
• Supervise transportation, import and export of products and supplies.
• Organize and supervise unused products and supplies destruction

- Responsible for Study start up activities, including: collacting, preparing and manteining (SIP) Documents.- Coordinate IRB/IEC submission, colect, track & review of appropiate clinical Documents to support regulatory Documents.- ensure accurancy of clinical site informatiion in databases (e-Clinical & CDSS) - Ensure patients informed consent forms are.

• Imports, export and distribution of clinical trial material, checking the receipt, warehousing, package, delivering to external and internal customers.
• Support in the trials, site selection, training, monitoring, data and clinical trial material management
• Warehouse systems support, Development of procedures related to CT material attached to GMP´s, GCP´s.
• Logistic area coordination and cleaning staff Support to clinical research protocols, handling and distributing CT material related.
• Material return and deletion according to regulatory, coordinating the material liberation processes in customs, Deviation reports.
• Proposal to increase the whorehouse of CR area, Store warehouse documentation according to GMP’s, ERP’s systems handling.

Master Project Supply Chain Management, Master Project Supply Chain Management

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