Analyst II eSource Data Acquisition Expert

Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Clinical Data Management
Job Category:
Professional
All Job Posting Locations:
Seoul, Korea, Republic of
Job Description:

About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://https://www.jnj.com/innovative-medicine

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
High Wycombe, United Kingdom - Requisition Number: R-006836
Seoul, Korea - Requisition Number: R-007021
Beerse, Belgium - Requisition Number: R-006299
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

Johnson & Johnson Innovative Medicine is recruiting for an Analyst II Esource Data Acquisition Expert to join our Data Acquisition-eSource team within the Integrated Data Analysis and Reporting (IDAR) Data Management & Central Monitoring organization.

Position Summary
Are 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 Data Acquisition-eSource team, the Analyst II Esource Data Acquisition Expert uses in-depth knowledge of electronic data capture build and design, data transfer specifications, (e.g. requirements gathering and creation), and integration testing to support a diverse clinical development portfolio. This role uses knowledge of industry standards and specifications for ingestion, transformation, and storage of external data.
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
• Evaluate electronic case report form build for compatibility with external data interoperability to create an integration specification
• 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, 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.
• Electronic data capture systems build and design
• Good understanding of the overall drug development process and GCP/ICH guidelines.
Preferred:
• Certified Electronic Data Capture builder
• Demonstrated understanding of relevant data collection, transfer, and submission industry standards (e.g., LOINC, ODM, HL7 FHIR®).
• Experience working with data from EHR/EMR, Digital Health technologies, and/or Real-World Data.