Senior Clinical Programming Lead - CDMX

Johnson & Johnson; Ciudad de México; Presencial; MXN 700,000 - 900,000; Jornada completa

Descripción de la vacante

A leading healthcare company is seeking a Senior Programming Lead in Mexico City. This role demands strong programming skills, particularly in SAS, along with experience in clinical data management and project oversight. The successful candidate will lead programming trial activities and collaborate with various stakeholders to enhance processes. A bachelor's degree in a relevant field and at least 4 years of experience are required. This position will contribute significantly to innovative healthcare solutions.

Formación

• 4+ years programming or clinical data management experience.
• Expert knowledge of CDISC Standards.
• Experience leading teams and vendor management oversight.

Responsabilidades

• Lead trial activities with technical expertise and oversight.
• Develop relationships with stakeholders for process improvements.
• Coordinate programming activities across teams.

Conocimientos

SAS

R

Python

Project management

Educación

Bachelor’s degree in computer science or related field

Herramientas

Data manipulation tools

Descripción del empleo

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

Mexico City, Mexico

Job 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.

• 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&SP activities.

Education and Experience Requirements

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.