Specialist Data Acquisition Expert - Antwerpen, België - Johnson & Johnson

Johnson & Johnson
Johnson & Johnson
Geverifieerd bedrijf
Antwerpen, België

1 maand geleden

Sophie Dubois

Geplaatst door:

Sophie Dubois

beBee Recruiter
Beschrijving

Janssen Research and Development, L.L.C., a member of Johnson and Johnson's Family of Companies, is recruiting for a
Specialist Data Acquisition Expert - External Data to join our
Data Acquisition & Coding (DAC) team within
Integrated Data Analysis and Reporting (IDAR) Data Management .

This position can be located in Beerse, Belgium; Leiden, Netherlands; Allschwil, Switzerland; remote flexibility may be considered.


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
Specialist Data Acquisition Expert - External Data , uses in-depth knowledge on the collection, ingestion, transformation, and storage of External Data to support a diverse clinical development portfolio.


In this role, you will:

  • Collaborate crossfunctionally and with external data providers to understand the purpose of data collected, align data availability and consumption requirements, and drive optimal data acquisition solutions.
  • Analyze data and content from external data streams and propose efficient pathways to acquire and integrate relevant data.
  • Lead the development and setup of traditional and novel data streams and related documents of low to high complexity.
  • Participate in continuous improvement initiatives contributing to innovation and the maturation of an industry leading data acquisition capability.
  • Actively contribute to the shaping of the organization, improving reusability, efficiency, and consistency of DAC tools and processes across studies and therapeutic areas.

Qualifications:


Qualifications:


  • Bachelor's degree in Health Sciences, Clinical Data Management or other relevant scientific field or equivalent work experience is required.
  • Minimum of 5 years relevant experience within the Pharmaceutical, CRO or Biotech industry, or equivalent is required.
  • Experience working in a multifunctional 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.
  • Demonstrated experience working with external data providers, clinical data, and data structures within a clinical study/research setting is required.
  • Solid understanding of the overall drug development process and GCP/ICH guidelines is required.
  • Demonstrated understanding of relevant data collection, transfer, and submission industry standards (e.g., CDASH, SDTM, HL7 FHIR, ODM) is preferred.
  • Experience working with data from EHR/EMR, Digital Health technologies, and/or Real-World Data is preferred.
  • Deep expertise in specialized data streams (e.g., 'omics data, immunogenicity, flow cytometry, PK, biomarkers) is preferred.
We are an equal opportunity employer and value diversity at our company.

We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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