Clinical Programmer, Integrated Data Analytics and Reporting
Johnson & JohnsonAbout the role
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational SciencesJob Sub Function:
BiostatisticsJob Category:
Scientific/TechnologyAll Job Posting Locations:
Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of AmericaJob Description:
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://www.jnj.com/innovative-medicine
Johnson & Johnson Innovative Medicine is searching for the best talent for the position of Clinical Programmer to join our Integrated Data Analytics and Reporting team (IDAR). This is a hybrid position which will be based in either Spring House, PA, Titusville, NJ or Raritan, NJ. We have multiple openings for this position.
Position Summary:
The Clinical Programmer is an individual contributor with knowledge of data structures, industry standards, programming languages, and programming methods. This role supports data analyses and reporting activities within trial activities in accordance with departmental processes and procedures.
This position is a member of the programming team, capable of supporting programming activities of one or more trials of low to medium complexity/criticality and may contribute to departmental innovation and process improvement projects.
Principal Responsibilities:
- Completes and may lead programming trial activities of low to medium complexity and/or criticality, with high quality and timeliness of deliverables.
- Accountable for the design and development of programs in support of clinical research analysis and reporting.
- Performs appropriate level of verification of programming and reporting activities. Reviews and provides input for project requirements and documentation.
- Supports submission activities including but not limited to creation, verification, and delivery of CDISC compliant and/or non-standard data packages and reviewer’s guides.
- Follows departmental processes and procedures, ensures use of latest standards and deployment of current technologies.
- May contribute to departmental innovation and process improvement projects.
- Collaborates effectively with team and cross-functional members.
- Ensures continued compliance with required company and departmental training, time reporting and other business/operational processes as required for position.
- Reviews specifications for mapping internal Data Review Model (DRM) for fit-for-purpose reporting consumption and ensures verification of DRM.
- Supports data cleaning by programming edit checks and data review listings and data reporting by creating data visualizations and listings for data management, medical monitoring, and central monitoring.
Principal Relationships:
- This role reports into a people manager position within the Delivery Unit and is accountable to the Portfolio and Study Leads for assigned activities and responsibilities.
- Functional contacts within IDAR include but are not limited to: Leaders and leads in Data Management and Central Monitoring, Programming Leads, Clinical Data Standards, Regulatory Medical Writing Leads, and system support organizations.
- Functional Contacts within J&J Innovative Medicine (as collaborator or peer) include but are not limited to: Statistics, Clinical, Global Medical Safety, Project Management, Regulatory, Strategic Partnerships, Human Resources.
- External contacts include but are not limited to external partners, CRO management and vendor liaisons, industry peers and working groups.
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