Clinical Programmer, Integrated Data Analytics and Reporting

Johnson & Johnson•Spring House, PA

39d•$89,000 - $143,750•Hybrid

About The Position

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.

Requirements

Bachelor's degree or higher and/or equivalent in computer science, data science/data engineering, mathematics, public health, or another relevant scientific field (or equivalent theoretical/technical depth).
At least 2 years of relevant programming experience, preferably in Pharmaceutical, CRO or Biotech industry or related field or industry.
Basic knowledge of regulatory guidelines (e.g. ICH-GCP) and relevant clinical R&D concepts.
Experience working in a team environment preferred.
Excellent written and verbal communications skills.
Knowledge of data structures and relevant programming languages for data manipulation/statistical analysis and reporting. May include SAS, R, Python, etc. SAS knowledge is preferred for Clinical Programming role.
Basic knowledge of processes, methods, and concepts relevant to programming.
This position offers the hybrid option and will be based in either Spring House, PA, Titusville, NJ or Raritan, NJ. (No fully remote option available for this role.)

Nice To Haves

Advanced Analytics
Analytical Reasoning
Biological Sciences
Biostatistics
Clinical Trials
Data Modeling
Data Privacy Standards
Data Quality
Data Savvy
Detail-Oriented
Good Clinical Practice (GCP)
Report Writing
Research Ethics
Researching
Statistical Analysis Systems (SAS) Programming
Statistics
Technologically Savvy

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.

Benefits

Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
Employees may be eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
Vacation - up to 120 hours per calendar year
Sick time - up to 40 hours per calendar year
Holiday pay, including Floating Holidays - up to 13 days per calendar year of Work, Personal and Family Time - up to 40 hours per calendar year

Stand Out From the Crowd

Upload your resume and get instant feedback on how well it matches this job.

Upload and Match Resume