Johnson & Johnson companies are equal opportunity employers.
Associate Scientific Director, Drug Development Information Governance (DDIG)-00000NAW
Description
Janssen Research & Development, L.L.C., a Johnson & Johnson company, is recruiting a Associate Scientific Director (lead) for the Drug Development Information Governance (DDIG) Initiative to be located in Spring House, PA; Titusville, NJ; Raritan, NJ or Beerse, Belgium.
Janssen Research & Development, L.L.C. develops treatments that improve the health and lifestyles of people worldwide. Research and development areas encompass novel targets in neurologic disorders, gastroenterology, oncology, infectious disease, diabetes, hematology, metabolic disorders, immunologic disorders, and reproductive medicine.
Janssen Pharmaceuticals, Inc., a pharmaceutical company of Johnson & Johnson, provides medicines for an array of health concerns in several therapeutic areas, including: attention deficit hyperactivity disorder (ADHD), cardiovascular disease, general medicine (acid reflux disease, infectious diseases), mental health (bipolar I disorder, schizophrenia), neurologics (Alzheimer’s disease, epilepsy, migraine prevention and treatment), pain management, and women’s health. Our ultimate goal is to help people live healthy lives. We have produced and marketed many first-in-class prescription medications and are poised to serve the broad needs of the healthcare market – from patients to practitioners, from clinics to hospitals. For more about Janssen Pharmaceuticals, Inc., one of the Pharmaceutical Companies of Johnson & Johnson, visit www.janssenpharmaceuticalsinc.com
The Associate Scientific Director, DDIG is responsible for defining, obtaining approval, and managing policies (terms and definitions, ownership, business rules, data lifecycle management) governing master data across drug development, in strong partnership with business functions. The successful candidate will also manage the design, build, and maintenance of the Master Data Domains and partner with IT for the development and maintenance of the technical Master Data Management (MDM) solution. Will drive the implementation of master data in drug development business processes and systems to reduce or eliminate compliance risk, create consistency and create business value. The DDIG lead drives agreement on how to align master data consistently across the functional areas in Janssen R&D
Will stay abreast of industry data standards; evaluating impact of changes and applicability for DDIG Master Data Domains and collaborate with a network of functional domain experts and data owners in the various business functions on industry standards. Will create and maintain appropriate metrics to represent the contents and the MDM operations for that domain and identify and elaborate on focus areas for improvement. Will bridge the master data needs from business processes supported by systems of use with the policies governing the master data in the MDM hub and the systems of record. Be a member of the Information Governance Center of Excellence (as part of the overall governance structure) and provide expertise to data related projects within the organization.
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer.
Qualifications
A Bachelor’s degree and a minimum of 8 years’ related experience is required OR a Master’s degree and a minimum of 5 years’ experience is preferred.
Knowledge and experience in one drug development business related area (Pre-clinical Development,
Clinical Development, Pharmaceutical Development and Manufacturing Sciences, Chemistry (small molecules) or Biology (large molecules), Medical Safety, Regulatory affairs and/or Quality and Compliance) is required.
Practical knowledge in Master Data Management with related business analysis and data modeling experience is required.
Business analysis and some data modeling experience is required.
Informatica MDM Hub, including Data Director and Data Quality tool experience is a plus.
Ability to thrive in a global multicultural, cross functional matrix environment is required.
Ability to manage high workload and critical issues in a timely matter is required.
Up to 10% travel is required.
BE VITAL in your career, Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies
Primary Location:North America-United States-New Jersey-Titusville
Other Locations:North America-United States-Pennsylvania-Spring House, North America-United States-New Jersey-Raritan, Europe/Middle East/Africa-Belgium-Antwerp-Beerse
Organization: Janssen Research & Development, LLC. (6084)
Job Function: R&D
Certain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
Johnson and Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status, or any other characteristic protected by law.
EEO is the Law
EEO is the Law GINA Supplement
Associate Scientific Director, Drug Development Information Governance (DDIG)-00000NAW
Description
Janssen Research & Development, L.L.C., a Johnson & Johnson company, is recruiting a Associate Scientific Director (lead) for the Drug Development Information Governance (DDIG) Initiative to be located in Spring House, PA; Titusville, NJ; Raritan, NJ or Beerse, Belgium.
Janssen Research & Development, L.L.C. develops treatments that improve the health and lifestyles of people worldwide. Research and development areas encompass novel targets in neurologic disorders, gastroenterology, oncology, infectious disease, diabetes, hematology, metabolic disorders, immunologic disorders, and reproductive medicine.
Janssen Pharmaceuticals, Inc., a pharmaceutical company of Johnson & Johnson, provides medicines for an array of health concerns in several therapeutic areas, including: attention deficit hyperactivity disorder (ADHD), cardiovascular disease, general medicine (acid reflux disease, infectious diseases), mental health (bipolar I disorder, schizophrenia), neurologics (Alzheimer’s disease, epilepsy, migraine prevention and treatment), pain management, and women’s health. Our ultimate goal is to help people live healthy lives. We have produced and marketed many first-in-class prescription medications and are poised to serve the broad needs of the healthcare market – from patients to practitioners, from clinics to hospitals. For more about Janssen Pharmaceuticals, Inc., one of the Pharmaceutical Companies of Johnson & Johnson, visit www.janssenpharmaceuticalsinc.com
The Associate Scientific Director, DDIG is responsible for defining, obtaining approval, and managing policies (terms and definitions, ownership, business rules, data lifecycle management) governing master data across drug development, in strong partnership with business functions. The successful candidate will also manage the design, build, and maintenance of the Master Data Domains and partner with IT for the development and maintenance of the technical Master Data Management (MDM) solution. Will drive the implementation of master data in drug development business processes and systems to reduce or eliminate compliance risk, create consistency and create business value. The DDIG lead drives agreement on how to align master data consistently across the functional areas in Janssen R&D
Will stay abreast of industry data standards; evaluating impact of changes and applicability for DDIG Master Data Domains and collaborate with a network of functional domain experts and data owners in the various business functions on industry standards. Will create and maintain appropriate metrics to represent the contents and the MDM operations for that domain and identify and elaborate on focus areas for improvement. Will bridge the master data needs from business processes supported by systems of use with the policies governing the master data in the MDM hub and the systems of record. Be a member of the Information Governance Center of Excellence (as part of the overall governance structure) and provide expertise to data related projects within the organization.
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer.
Qualifications
A Bachelor’s degree and a minimum of 8 years’ related experience is required OR a Master’s degree and a minimum of 5 years’ experience is preferred.
Knowledge and experience in one drug development business related area (Pre-clinical Development,
Clinical Development, Pharmaceutical Development and Manufacturing Sciences, Chemistry (small molecules) or Biology (large molecules), Medical Safety, Regulatory affairs and/or Quality and Compliance) is required.
Practical knowledge in Master Data Management with related business analysis and data modeling experience is required.
Business analysis and some data modeling experience is required.
Informatica MDM Hub, including Data Director and Data Quality tool experience is a plus.
Ability to thrive in a global multicultural, cross functional matrix environment is required.
Ability to manage high workload and critical issues in a timely matter is required.
Up to 10% travel is required.
BE VITAL in your career, Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies
Primary Location:North America-United States-New Jersey-Titusville
Other Locations:North America-United States-Pennsylvania-Spring House, North America-United States-New Jersey-Raritan, Europe/Middle East/Africa-Belgium-Antwerp-Beerse
Organization: Janssen Research & Development, LLC. (6084)
Job Function: R&D
Certain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
Johnson and Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status, or any other characteristic protected by law.
EEO is the Law
EEO is the Law GINA Supplement