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
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
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
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
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
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
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