Senior Clinical Programming Lead

hace 3 semanas

América, México Johnson & Johnson A tiempo completo

**Job Function**:Data Analytics & Computational Sciences**Job Sub Function**:Biostatistics**Job Category**:Scientific/Technology**All Job Posting Locations**:Mexico City, Mexico**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**: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.

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