Senior Global Dictionary Analyst.
☞ The Janssen Pharmaceutical Companies of Johnson & Johnson
Visualizza: 215
Giorno di aggiornamento: 29-03-2024
Località: Basel-Landschaft BL Allschwil
Categoria: I saldi
Industria: Medical Equipment Manufacturing Hospitals Health Care Pharmaceutical Manufacturing
Tipo di lavoro: Full-time
Contenuto del lavoro
Janssen Research and Development, L.L.C., a member of Johnson and Johnson’s Family of Companies, is recruiting for a Senior Global Dictionary Analyst to join our Data Acquisition & Coding (DAC) team within Integrated Data Analysis and Reporting (IDAR) Data Management.This position is to be located in Springhouse, PA; Chesterbrook, PA; Titusville, NJ; Raritan, NJ; High Wycombe, UK; Beerse, Belgium; Leiden, Netherlands; Allschwil, Switzerland; remote flexibility may be considered in the countries listed.
At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at www.janssen.com and follow us @JanssenGlobal. Janssen Research & Development, LLC is part of the Janssen Pharmaceutical Companies.
Diversity & Inclusion are crucial to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions!
Are you ready to join a growing team driving the implementation of data acquisition strategy and the future e-clinical trial landscape at Janssen R&D?!
As a key member of the DAC team, the Senior Global Dictionary Analyst, assists in the provision of multi-functional support in coding governance and associated processes.
You will be responsible for enabling the provision of consistent, accurate and reproducible coding of clinical study data, and ensure adherence to established Janssen coding processes and guidelines by DM CRO vendors.
You will contribute to global thesaurus and code list maintenance, along with the maintenance and enhancement of dictionary encoding products and systems.
The successful candidate will work in an agile, fast paced, highly motivated, team centric and evolving data environment. You will apply creative problem-solving skills and knowledge to support R&D innovation.
In This Role, You Will
- Provide oversight of IDAR data coding activities to ensure adherence to Regulatory Authority and Industry standards for coding practices and processes.
- Execute and promote adherence to established coding governance activities and principles.
- Support delivery of consistent, accurate and reproducible coding of clinical trial data meeting individual project timelines.
- Knowledge sharing of coding processes and coding encoding systems with cross‐functional colleagues.
- Address cross‐functional and cross‐sectoral coding inquiries and data coding issues.
- Participate in continuous improvement initiatives contributing to innovation and the maturation of an industry leading data acquisition and coding capability.
- Actively contribute to the shaping of the organization, improving re-usability, efficiency, and consistency of coding tools and processes across studies and therapeutic areas.
- Bachelor’s degree in Health Sciences, Nursing, or other relevant scientific field, or equivalent work experience is required.
- Minimum of 3 years relevant experience within the Pharmaceutical, CRO or Biotech industry, or equivalent is required.
- Proven knowledge of industry standard coding thesauri (MedDRA, WHO Drug) and the ability to use and contribute to the maintenance of incumbent dictionary encoding products and systems is required.
- Experience working in a multi-functional environment and ability to adapt to different ways of working is required.
- Proven track record of effective communication skills, including strong verbal and written communication, influencing, and partnering skills is required.
- Detailed understanding of the overall drug development process and GCP/ICH guidelines is preferred.
- #GIFTS
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Primary Location
United States-Pennsylvania-Spring House-Welsh & McKean Roads
Other Locations
Europe/Middle East/Africa-United Kingdom-England-High Wycombe, North America-United States-New Jersey-Titusville, North America-United States-Pennsylvania-Chesterbrook, Europe/Middle East/Africa-Switzerland-Allschwil, Europe/Middle East/Africa-Netherlands, Europe/Middle East/Africa-Switzerland, Europe/Middle East/Africa-United Kingdom, North America-United States-New Jersey-Raritan, Europe/Middle East/Africa-Belgium-Antwerp-Beerse, Europe/Middle East/Africa-Belgium, Europe/Middle East/Africa-Netherlands-South Holland-Leiden, North America-United States
Organization
Janssen Research & Development, LLC (6084)
Job Function
R&D
Requisition ID
2206004671W
Scadenza: 13-05-2024
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