Clinical Logistics Manager I

Job Category: Biotech/R&D/Science Career Level: Experienced (Non-Manager) Location: Lowell, MA 01851           Job Description: PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, medical marketing and consulting services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement. Headquartered near Boston, Massachusetts, PAREXEL operates in 55 locations throughout 43 countries around the world, and has over 6,315 employees. For more information about PAREXEL International visit www.PAREXEL.com Essential Functions:The Clinical Logistics Manager I (CLM I) elaborates and conducts logistics processes for clinical trials to the highest standards of quality and efficiency, ensuring that projects are conducted according to quality standards, including standard operating procedures, ICH, GCP, and GMP.Relationships:Reports To: Functional Manager, Clinical Logistics ServicesDirectly Supervises: Clinical Logistics Assistants, as applicableWorks Closely With: Other Clinical Logistic Services employees, Project Managers, Clinical Research Associates, IVRS personnel, Regulatory Consultants, Data Managers, Statistical Programmers, Medical Services, Sales / Business Development, Finance.External Relationships: Sponsors, investigators, third-party contractors.Responsibilities:' Support for development of logistics strategy for specific CLS service offerings (Clinical Trial Supply, Lab Logistics, Ancillary Supply).' Identification, qualification, and management of third-party contractors, as appropriate.' Organization of specific import / export activities across countries / states.' Participation in and organization of documentation development, in support of CLS service delivery.' Control of GMP compliance in collaboration with Quality.' Supervision of specific third-party services in collaboration with Investigators, Clinical Research Associates, and service providers.' Participation in team meetings, as required.' Control and report of costs for internal service fees as well as third-party service providers for activity supervised.' Use of positive, objective, balanced, and result-driven approach. Education:' Bachelor degree, or equivalent (e.g. Pharm. D.), in biology, pharmacy, or other health-related discipline.Minimum Work Experience:' Two years of experience in clinical logistics or related field within the biopharmaceutical industry.' International work experience a strong plus. Skills: ' Ability to build rapport with a culturally diverse group at multiple levels and disciplines.' Credible team player with good facilitation skills. ' Result-oriented, confident, self-motivated, and driven / high energy.' Solid communication (verbal & written) and negotiation skills. Ability to influence and gain collaboration from and respect of key stakeholders. ' Good analytical capabilities combined with creative problem-solving skills and a sense of urgency. ' Flexible, capable of managing change and ambiguity.' Understanding of business financial metrics.' Strong client focus.' Good knowledge of Microsoft Office programs (Word, PowerPoint, and Excel).' Demonstrated ability to conduct business in English (written and spoken) and in local language if different from English.' Knowledge of Foreign language(s) a plus. RESPOND HERE! Respond immediately by accessing the following dedicated online response form which will allow you to cut and paste your resume. This form will go directly and immediately to the hiring authority for this position. Access the online response form at: http://sh.webhire.com/servlet/resp/rf?jobid=2217155&boardid=749