Are you a highly skilled and experienced statistical programmer looking for an exciting new opportunity? Novartis is seeking a Senior Principal Statistical Programmer to join our dynamic team and help drive innovation in pharmaceutical research and development. In this role, you will have the opportunity to utilize your expertise in statistical programming to support cutting-edge clinical trials and contribute to the advancement of new therapies for patients worldwide. We are looking for a dedicated and driven individual with a strong background in statistical programming, excellent problem-solving skills, and a passion for making a difference in the healthcare industry. If this sounds like you, we invite you to apply and be a part of our mission to reimagine medicine.
Develop and implement statistical programming strategies for clinical trials and drug development projects.
Collaborate with cross-functional teams to ensure efficient and high-quality statistical programming deliverables.
Utilize advanced statistical programming techniques and tools to analyze and interpret clinical trial data.
Generate and validate analysis datasets, tables, listings, and figures for clinical study reports.
Review and provide input on statistical analysis plans and study protocols.
Ensure compliance with regulatory guidelines and company standard operating procedures.
Identify and troubleshoot issues related to statistical programming and propose solutions.
Mentor and train junior statistical programmers on advanced programming techniques and processes.
Stay updated on industry trends and advancements in statistical programming methods and tools.
Contribute to the continuous improvement of processes and tools to enhance efficiency and quality.
Participate in cross-functional meetings and provide input on statistical programming aspects of clinical trials.
Communicate effectively with internal and external stakeholders to ensure alignment and timely delivery of statistical programming deliverables.
Act as a subject matter expert for statistical programming and provide guidance to project teams.
Proactively identify opportunities for process improvement and contribute to the development and implementation of best practices.
Adhere to project timelines and prioritize tasks to meet project deliverables and milestones.
Take ownership of assigned projects and ensure all programming activities are completed on time and within budget.
Maintain accurate and organized documentation of programming activities.
Comply with all company policies and procedures related to data integrity and confidentiality.
Act as a role model for the team by demonstrating a strong work ethic, professionalism, and a positive attitude.
Uphold the company’s mission and values while contributing to the advancement of new therapies for patients worldwide.
Where is this job?
This job is located at Dublin, Ireland
Job Qualifications
Advanced Programming Skills: A Senior Principal Statistical Programmer At Novartis Should Have Strong Expertise In Sas Programming And Other Statistical Software Such As R Or Python. They Should Be Able To Develop Complex Programs And Macros For Data Manipulation, Analysis, And Reporting.
Extensive Clinical Trial Experience: The Ideal Candidate Should Have At Least 10 Years Of Experience In The Pharmaceutical Industry, With A Strong Focus On Clinical Trial Programming. They Should Have A Thorough Understanding Of The Drug Development Process And The Ability To Work With Large And Complex Datasets.
Leadership And Team Management: As A Senior Member Of The Team, The Candidate Should Have Excellent Leadership Skills And The Ability To Manage A Team Of Statistical Programmers. They Should Be Able To Mentor And Train Junior Programmers, As Well As Provide Guidance And Support To Cross-Functional Teams.
Regulatory Knowledge: A Senior Principal Statistical Programmer Should Have A Deep Understanding Of Regulatory Requirements And Industry Standards, Such As Cdisc And Ich Guidelines. They Should Be Able To Ensure That All Programming Activities Are In Compliance With These Regulations And Standards.
Strong Communication And Collaboration Skills: The Candidate Should Possess Excellent Communication Skills And The Ability To Collaborate Effectively With Cross-Functional Teams, Including Biostatisticians, Data Managers, And Clinical Teams. They Should Also Have Experience In Presenting Complex Statistical Information To Non-Technical Stakeholders.
Required Skills
Data Management
Statistical Modeling
SAS Programming
Statistical Programming
Team Leadership
Database Design
Data Interpretation
FDA Regulations
Project
Clinical Trials
Clinical Data Analysis
Statistical Reporting
Soft Skills
Communication
Conflict Resolution
Leadership
Time Management
Creativity
Teamwork
Adaptability
Problem-Solving
Empathy
Decision-Making
