Title: Clinical Database Manager Location: Montvale, NJ Duration : Fulltime
Responsible for clinical aspects associated with all internally developed PDR content including the aggregation and ongoing maintenance of the PDR Labeling Compendium consisting of FDA Approved Product Information covering 99% of the prescriptions dispensed in the U.S. Manage the content development operation by overseeing offshore vendor and onshore staffing to ensure all content sets are accurate, up-to-date and meet defined service level requirements for PDR clients. Define appropriate nomenclature and implement common taxonomy across all content sets (Concise, Consumer, PDR Labeling Data) to optimize usability of content and facilitate the creation of new digital offerings. Define functional specifications, implement and monitor system enhancements required to ensure effective content management . Essential Duties/Responsibilities Define and implement common clinical nomenclature/taxonomy and integrate across all content sets (databases/applications). Maximize the use of industry standards (e.g. SNOMED) selectively across all content sets in a manner which maximizes opportunities for repurposing and licensing of data. Develop and document editorial guidelines and standard operating procedures associated with indexing, coding and abstracting drug labeling information. Implement a workflow which ensures that all PDR drug content sets are updated on a synchronized schedule. Train and oversee offshore vendor and onshore permanent and temporary staff responsible for creating and maintaining all PDR content sets and associated index data. Accountable for the performance of offshore vendor and on-shore support staff. Develop, maintain and monitor key metrics. Ensure content set updates are scheduled and managed as necessary to ensure on time launch of new mobile offering and subsequent releases as well as rollout and maintenance of PDR Drug Information Service to pharmaceutical customers. Act as the clinical lead on a project team responsible for implementing a document management capability. Review and recommend changes to existing systems as necessary to ensure most efficient and error-free maintenance of data. Includes writing functional specifications and implementing same. Provide clinical support to product management, business development, sales and client services. Manage off shore resources Manage on-site temporary staff Directly supervise drug information specialist. Directly supervised by Director of Clinical Services Required Knowledge, Skills and Attributes Incumbent needs to be proactive with the proven ability to manage multiple tasks simultaneously. Must be a highly organized. Good analytical skills with the ability to quickly understand and assimilate various data points and make qualified judgments around courses of action. Must be able to communicate effectively across various departments within the company. Required Education and/or Experience Pharm D Required 1 - 3 years management experience. Must have prior Healthcare experience Must have drug information and database experience - Location: Montvale, NJ - Compensation: As per the market - Principals only. Recruiters, please don't contact this job poster. - Please, no phone calls about this job! - Please do not contact job poster about other services, products or commercial interests. --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "java-core" group. To post to this group, send email to [email protected] To unsubscribe from this group, send email to [email protected] For more options, visit this group at http://groups.google.co.in/group/java-core?hl=en-GB -~----------~----~----~----~------~----~------~--~---
