Senior Clinical Programming Lead

Johnson & Johnson Innovative Medicine; Xico; Presencial; MXN 1,454,000 - 1,818,000; Jornada completa

Descripción de la vacante

A global healthcare company in Veracruz is seeking a Senior Programming Lead to oversee programming trial activities. The ideal candidate will possess a Bachelor's degree in a scientific field and have at least 4 years of experience in programming and clinical data management. Proficiency in SAS and knowledge of CDISC standards are essential. The role involves planning, decision-makers, and improving efficiency in programming functions within clinical trials.

Formación

• 4+ years programming and or clinical data management experience.
• Knowledge of programming practices and tools.
• Experience in planning and coordinating programming activities.

Responsabilidades

• Provide expertise, planning, and oversight of programming trial activities.
• Make decisions impacting efficiency and quality of deliverables.
• Develop cross‑functional working relationships with stakeholders.

Conocimientos

Programming and data management experience

Knowledge of SAS

Expert CDISC Standards knowledge

Proficiency in Python

Project management skills

Regulatory guidelines knowledge

Educación

Bachelor's degree in relevant scientific field

Herramientas

SAS

R

Python

Descripción del empleo

Company Overview

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.

Job Information

Learn more at Job Function : Data Analytics & Computational SciencesJob Sub Function : BiostatisticsJob Category : Scientific / TechnologyAll Job Posting Locations : Mexico City, MexicoJob Description : Position Summary : The Senior Programming Lead is an experienced programmer with an advanced knowledge of programming languages, has expertise in industry standards, complex data structures and programming methods, having the technical capabilities in leading trial activities in accordance with departmental processes and procedures.

Position Summary

The Senior Programming Lead is an experienced programmer with an advanced knowledge of programming languages, has expertise in industry standards, complex data structures and programming methods, having the technical capabilities in leading trial activities in accordance with departmental processes and procedures.

Responsibilities

• This role is responsible for providing expertise, planning and oversight of one or more programming trial activities of moderate to high complexity.
• The role makes decisions and recommendations that impact the efficiency, timeliness, and quality of deliverables, and provides leadership, direction, and technical guidance to programming teams.
• This role develops cross‑functional working relationship with stakeholders to shape processes and practices and contributes expertise to Delivery Unit or departmental innovation and process improvement projects.
• The Senior Programming Lead position combines the expertise and responsibilities in their respective programming roles, making them an asset to IDAR's C&S activities.

Education and Experience Requirements

• Bachelor's degree or higher and / or equivalent in computer science, mathematics, data science / analytics / data engineering, public health, or other relevant scientific field (or equivalent theoretical / technical depth).

Experience and Skills Required

• Approx. 4+ years programming and or clinical data management experience with increasing responsibility preferably in pharmaceutical / clinical trial environment.
• Knowledge of programming practices (including tools and processes).
• Knowledge of data structures and relevant programming languages for data manipulation / statistical analysis and reporting. May include SAS, R, Python, etc.
• Knowledge of SAS is required.
• Expert CDISC Standards knowledge.
• Experience in planning and coordinating programming activities and leading teams.
• Experience working with cross functional stakeholders and teams.
• Experience in vendor management oversight.
• Project management skills and knowledge of team management principles.
• Working knowledge of regulatory guidelines (e.g. ICH-GCP) and relevant clinical R&D concepts.
• Demonstrated written and verbal communication skills.