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About the Role

The Experienced Programmer 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.

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.

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).
Approx. 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.
Basic knowledge of processes, methods, and concepts relevant to programming.

Skills

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
SAS
R
Python

Location

Chiyoda, Tokyo, Japan

Work Type

Full-time

Experience Level

Experienced

Education Level

Bachelor's degree or higher

About the Company

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 jnj.com.
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.