Clinical Programmer, Integrated Data Analytics and Reporting

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 Sciences

Job Sub Function:
Biostatistics

Job Category:
Scientific/Technology

All Job Posting Locations:
Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America

Job 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...