Sr Clinical Logistics Analyst - (US-MA-Cambridge - 02239)

Minimum Education: None
Job Type: Full Time
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Responsibilities: Scientific excellence that achieves new standards of care drives the company's work. Over 20 products are currently in clinical development addressing a variety of key medical needs. In addition to 's promising portfolio of drug candidates, the company's capabilities and capacity for protein manufacturing are world-class in quality and scale. The company is one of a handful of biotechnology companies that has three licensed and dedicated biological bulk-manufacturing facilities, including its large-scale manufacturing plant in Research Triangle Park, NC, which is one of the world's largest cell culture facilities. An additional large-scale manufacturing plant is under construction in Hillerød, Denmark. Founded in 1978, is a global leader in the discovery, development, manufacturing and commercialization of innovative therapies. Patients in more than 90 countries benefit from 's significant products that address diseases such as multiple sclerosis (MS), lymphoma and rheumatoid arthritis. In 2008, 's total revenues surpassed $4 Billion. The company currently employs approximately 4,700 people worldwide. Management of clinical finished goods distribution to US and international depot locations and clinical sites. Primary responsibilities of the position are: - Monitoring of clinical order process/fulfillment as executed by 3rd party distributors - Raise order fulfillment issues to management and key customers and propose mitigation strategies on a routine (daily/weekly) basis - Foster a positive working relationship between and the contracted distributors used for the trial protocols managed by this individual - Involvement in distribution operational aspects of clinical trial setup in relation to IVRS programming strategy, IVRS report types, available shipping day algorithms, depot selection process, courier selection, shipping box type approval, incoming bulk receipts and compilation of data for performance metrics population - Primary contact for internal customers (clinical Operations, clinical planning, QA) and the distribution vendors for all distribution related topics for the trial protocols responsible for - Responsible for documentation of processing deviations and subsequent investigation authoring, CAPA implementation - Generation of purchase orders and approval of invoices related to managed trials based on budget detailsRequirements: - Strong written and oral communication skills - Ability to multitask on a daily basis and maintain multiple projects in parallel - Proven capability to work in a fast paced dynamic environment - Experience in a regulated industry or in an environment dealing with workflow industry contraints (i.e. ISO, ISTA, GMP, etc.) - Prior Logistics experience - Cold chain logistics or pharmaceutical logistics experience a plus Education: A Bachelor Degree in a technical discipline or Industrial Engineering is required.EducationSee Requirements: section above

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