Experienced I Statistical Programmer

Johnson & Johnson Innovative Medicine; Mumbai; On-site; INR 900,000 - 1,300,000; Full time

Job summary

Johnson & Johnson Innovative Medicine in Mumbai seeks an Experienced Programmer to support data analyses and reporting within clinical trial activities. You will contribute to the programming team, handling lower-to-medium complexity trials with quality and timeliness.

The role requires a bachelor’s degree and about 2+ years of coding experience in SAS, R or Python, with a basic grasp of regulatory guidelines and cross-functional collaboration.

Qualifications

• Bachelor’s degree or higher in computer science, data science/data engineering, mathematics, public health, or another relevant field.
• Approximately 2+ years of relevant programming experience in pharmaceutical, CRO or Biotech industry or related field.
• Knowledge of regulatory guidelines (e.g. ICH-GCP) and coding in SAS, R, Python.

Responsibilities

• Executes and may lead programming trial activities of low to medium complexity/criticality with high-quality deliverables.
• Designs and develops programs in support of clinical research analysis and reporting.
• Performs verification of programming and reporting activities and contributes to project documentation.
• Supports submission activities including creation, verification, and delivery of CDISC compliant and/or non-standard data packages and reviewer’s guides.
• Follows departmental processes and uses current technologies; collaborates with team and cross-functional partners.

Skills

SAS

R

Python

Teamwork

Communication

Education

Bachelor’s degree or higher in computer science or related field

Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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.

Job Sub Function

Biostatistics

Job Function

Data Analytics & Computational Sciences

Job Sub Function

Biostatistics

Job Category

Scientific/Technology

All Job Posting Locations

Bangalore, Karnataka, India, Mumbai, India, PENJERLA, Telangana, India

Job Description

Integrated Data Analytics and Reporting (IDAR)

Experienced Programmer (ST05)*

(*Title may vary based on Region or Country requirements)

Position Summary

The Experienced 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.

Clinical Programmer

• 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.

Education And Experience 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).

Experience And Skills Required

• 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. May include SAS, R, Python, etc. SAS knowledge is preferred for Clinical Programming role.
• Basic knowledge of processes, methods, and concepts relevant to programming.

Preferred 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