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Job Title: Senior Consultant, Regulatory Services
Job Location: PA: Horsham
Pay Rate: Open
Job Length: full time
Start Date: 2008-05-10

Company Name: Thomson Reuters
Contact: HR
Phone: email only please
Fax: email only please

Description: Thomson Reuters is a global leader in providing essential information to the world%%27s businesses and professionals in Law, Financial Services, Tax & Accounting, Media, Healthcare and Scientific Research. With our deep expertise and understanding of theses professions, we are able to offer our customers a broad range of innovative products and services. The relevant, insightful information and intuitive supporting systems we provide enable our customers to be successful. Thomson Reuters has operations in 93 countries around the globe. More information about Thomson Reuters and its financial performance can be found onwww.ThomsonReuters.com.

The Scientific business of Thomson Reuters provides information and knowledge to accelerate research, discovery and innovation. Our authoritative, accurate and timely information is essential for drug companies to discover new drugs and get them to market faster; researchers to find relevant papers and know what’s newly published in their subject; and businesses to optimize their intellectual property and find competitive intelligence. We will create the research platforms and services of the future that will power our customers toward business and personal success. The Senior Consultant leads project teams in the production of submissions and delivery of regulatory services in accordance with defined agency guidelines while balancing the quality and timeliness of customer deliverables.

* Provide advanced paper and electronic publishing services including document preparation, legacy conversion, scanning, rendering, bookmarking, hyperlinking, compilation, table of contents creation, volumation, pagination, and formatting of complex submissions. Prepare templates and set up submissions. * Perform quality assurance of published output for completeness and correctness in formatting and navigation. * Perform advanced document management tasks including file transfer, storage, tracking, and archival. * Maintain familiarity with current global regulatory submission standards. Contribute to departmental interpretations and best practices. * Maintain familiarity with and contribute to departmental standard operating procedures and work instructions. Write validation test scripts. * Provide project team leadership and manage publishing tasks. Initiate, plan, execute, control, and close assigned projects. Articulate procedures and solutions to multi-level team under time pressures imposed by business-critical deadlines. * Formulate and deliver presentations and workshops. Provide assistance to other departments including Consulting Services, Technical Support, Product Management, Sales, Education, and Regulatory Strategies as needed. Attend conferences and educate internal team on industry news. * Bachelor’s degree or equivalent in life sciences or technology-related discipline. Scientific Advanced Certified Publisher and/or Administrator Certification preferred. * Minimum of 3 years pharmaceutical industry experience. End-to-end regulatory submission publishing and document management experience required with minimum of 2-3 years CoreDossier, EZsubs, and/or InSight publishing and/or implementation. Leadership, project management, and public speaking experience preferred. * Understanding of global regulatory submission formats, industry standards, and guidelines, software validation concepts, and publishing best practices. * Effective oral and written communication to internal and external audiences; Above-average problem-solving, time management, analytical, adaptability, listening, negotiation, and leadership skills; Ability to work independently and in a team environment; Strong organizational and interpersonal skills with a customer service focus; Excellent attention to detail; Ability to work under pressure and adhere to deadlines. * Travel to and consistent presence at customer sites as needed to complete contracted services will be required. Up to 50%% travel potential.

The H-1B visa cap has been fulfilled for fiscal year 2008 which begins October 1, 2007 and therefore Thomson Reuters is unable to sponsor new (first-time) H-1B visas. Thomson Reuters employees take pride in providing our customers around the world with information that is timely, accurate, unbiased and trusted. We have a profound respect for the professions and customers we serve and define our success in terms of their success. Our work environment is dynamic, innovative and entrepreneurial. We have a result- oriented culture that demands excellence, agility and the desire to move quickly and precisely to seize opportunities. Our environment is both challenging and supportive — we give employees the opportunity to develop their skills and do their best work. Thomson Reuters values diversity of culture and thought, and seeks talented, qualified employees in all its operations around the world regardless of race, gender, national origin, religion, sexual orientation, disability, age or any other protected classification under country or local law. Thomson Reuters is proud to be an Equal Employment Opportunity/Affirmative Action Employer.

Please refer to Job code thomson-183820 when responding to this ad.

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