
Johnson & Johnson
Job title:
Analyst II Ext. Data Acquisition Expert
Company
Johnson & Johnson
Job description
Johnson & Johnson Innovative Medicine is currently seeking an Analyst II External Data Acquisition Expert to join our External Data Acquisition team within the Integrated Data Analysis and Reporting (IDAR) Data Management & Central Monitoring organization to be located in Beerse, Belgium; High Wycombe, United Kingdom; or Warsaw, PolandAre you ready to join a growing team driving the implementation of data acquisition strategy and the future e-clinical trial landscape at Johnson & Johnson?!As a key member of the External Data Acquisition team, the Analyst II External Data Acquisition Expert uses in-depth knowledge on the collection, ingestion, transformation, and storage of external data to support a diverse clinical development portfolio.You will be empowered to drive data acquisition activities for a portfolio of trials and data streams within assigned scope and serve as a subject matter expert on a variety of domains (e.g., non-CRF, Devices & Apps, Electronic Health Records (EHR), Direct Data Capture).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, staying abreast of relevant industry trends and innovative technologies related to external data.Key responsibilities
- Collaborate cross-functionally 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 within assigned scope.
- 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 re-usability, efficiency, and consistency of tools and processes across studies and therapeutic areas.
Qualifications – ExternalQualifications, skills, and experience
Required:
- Bachelor’s degree (e.g., BS, BA) or equivalent professional experience is required, preferably in Clinical Data Management, Health, or Computer Sciences. Advanced degrees preferred (e.g., Master, PhD).
- Minimum 2 years of experience in Pharmaceutical, CRO or Biotech industry or related field or industry.
- Experience working in a multi-functional environment and ability to adapt to different ways of working.
- Proven track record of effective communication skills, including strong verbal and written communication, influencing, and partnering skills.
- Demonstrated experience working with external data providers, clinical data, and data structures within a clinical study/research setting.
- Good understanding of the overall drug development process and GCP/ICH guidelines.
Preferred:
- Demonstrated understanding of relevant data collection, transfer, and submission industry standards (e.g., CDASH, SDTM, HL7 FHIR, ODM).
- Experience working with data from EHR/EMR, Digital Health technologies, and/or Real-World Data.
- Expertise in specialized data streams (e.g., ‘omics data, immunogenicity, flow cytometry, PK, biomarkers).
#LI-ŠJ1, #LI-Hybrid
Expected salary
Location
Beerse, Antwerpen
Job date
Wed, 05 Mar 2025 08:42:17 GMT
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