The U.S. Pharmacopeial Convention (USP) (Senior) Clinical Informatics Content Mgr in Rockville, Maryland
(Senior) Clinical Informatics Content Mgr
Research & Innovation
This hands-on individual contributor is responsible for product development, editing, and publishing, externally facing USP electronic drug databases and associated products. The individual will work in the new Digital & Innovation division on the Translational Informatics team, along with partners in Global Science and Standards and Global Information Services to ensure that USP delivers high quality digital content that can be integrated into hospital, pharmacy, drug wholesaler, and other Health IT implementations.
Roles and Responsibilities
Manage content of external facing USP datasets related to drug classifications and drug information
Ensures accurate maintenance of content through translational / ETL processes from compendial to machine-readable forms.
Works with technical and science teams to create requirements and/or enhance tooling for drug classifications as to ensure functional adequacy, scientific accuracy, and timely publication
Creates and documents editorial rules and SOPs as needed
Represents USP in relevant external meetings and committees with other consortiums, standards setting bodies, government agencies, etc.
Monitors external data sources for internal data alignment (e.g. USAN, FDA-approved drugs, RxNorm/DailyMed feeds)
Works with manager to develop and track progress along accurate project plans defining approach, timelines, and deliverables
Seeks and flags opportunities to enhance impact of existing data, including through integration with other internal or external data sets
Editorial and Content Manager
MS in Health Informatics, Computer science, Data Science, or a related field
Five (5) years of relevant experience in R&D lab, QA/QC lab, or software development in the appropriate domain
Senior Editorial and Content Manager
PhD. Pharmacy with MS in Health Informatics, Computer science, Data Science, or a related field
Five (5) years of relevant experience
Experience in creation and/or maintenance of private or public electronic drug databases that are used in Clinical Decision Support Systems (CDSS), Computerized Physician Order Entry (CPOE) systems, or similar clinical implementations
Experience in digital product quality assurance and data governance
Proficiency in customer, professional engagement in clinical realm
Experience in mapping/editing drug information to vocabulary standards such as RxNorm, UNII, FDA Establish Pharmacologic Classes (EPC), etc.
Experience in data quality and governance
Experience in using software to edit, version, publish, and evaluate quality of controlled terminologies and/or classifications
Experience in usage of data models and classifications in the drug domain such as MED-RT, ATC Classification, USP Drug Classification, etc.
Experience with tools such as Python, Unix, R Studio, Tableau, MySQL/Oracle, Protégé, or other tools and software as to query and analyze unstructured or structured data
Ability to communicate end-user requirements to software developers to enhance technical platforms
Ability to handle multiple priorities in a fast-paced environment.
Strong people skills and organizational skills
Excellent communications skills, including both verbal and written
Ability to present and impart knowledge to diverse audiences, including both technical and non-technical ones
USP offers an impressive benefits package , including:
Generous paid time off – 14 paid holidays, 10 sick days and 15 vacation days per year to start
An annual 401(k) contribution, beginning after 1 year of service, of 10% of pay (base and bonus) every pay period that vests immediately
Comprehensive individual and family healthcare plans with affordable premiums and low annual deductibles ($250/individual or $500/family)
The U.S. Pharmacopeial Convention (USP) is a scientific nonprofit organization that sets standards for the identity, strength, quality, and purity of medicines, food ingredients, and dietary supplements manufactured, distributed and consumed worldwide. USP’s drug standards are enforceable in the United States by the Food and Drug Administration, and these standards are used in more than 140 countries.
Being a part of USP means belonging to a diverse culture made up of more than 1,000 talented professionals working together at five international locations. We share our expertise in science, IT, human resources, quality assurance, communications, administrative management, and more...all to support an overall mission dedicated to making a difference by providing standards and programs that help improve the quality of medicines, dietary supplements, and foods worldwide.
USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. Employment selection and related decisions are made without regard to sex, race, age, disability, religion, national origin, color, veteran status, sexual orientation, gender identity or any other protected class. We are committed to working with and providing reasonable accommodation to individuals with disabilities.
USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.
Job Category Research & Innovation