We anticipate the application window for this opening will close on - 1 Dec 2025

 

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

The Cardiac Rhythm Management operating group is a division within Medtronic focused on developing and manufacturing medical devices and solutions for the management of cardiac arrhythmias and heart failure. This group’s product portfolio includes implantable pacemakers, implantable cardioverter-defibrillators (ICDs), cardiac resynchronization therapy (CRT) devices, and remote monitoring systems. CRM’s mission is to improve patient outcomes and quality of life by providing innovative therapies for the detection, prevention, and treatment of abnormal heart rhythms. The group collaborates closely with healthcare professionals and leverages advanced technology and data-driven insights to drive improvements in cardiac care.

At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary. 

This position will be based in Mounds View, MN.

In this exciting role as a Senior Statistical Programmer, the incumbent will leverage his/her knowledge and experience in statistical programming and device database skills to support all statistical programming activities in clinical studies. You will join a Statistical Programming team, as a part of the CRM Clinical Biostatistics and Data Science. Partnering with Statisticians, Data Management and Study Managers, the groups support clinical studies in CRM operating units and conduct efforts in data-based clinical evidence generation including and not limited to coordinating programming activities among the study programmers to achieve timely deliveries in the following areas: ADaM-like or analysis datasets, statistical tables, listings, and figures (TLFs), data reconciliation reports, and other internal and external reports. This role reports to the Sr. Manager, Statistics at Medtronic Cardiac Rhythm Management (CRM) operating units.

This role develops and validates statistical programs for creating analysis datasets, tables, figures, and listings, often for clinical trial submissions. This role involves leadership, technical expertise in programming languages like SAS, collaboration with statisticians and other teams, and ensuring compliance with standards such as CDISC. The position requires problem-solving, project management, and technical support to meet project deadlines and quality standards

Responsibilities may include the following and other duties may be assigned.

• Designs, plans, and executes Statistical Programming components of plans for clinical projects that establish the conditions essential for determining safety, efficacy, and marketability of medical device products.
• Uses sound statistical programming terminology to conduct studies relating to the life cycle of the product.
• Responsible for creating programs to develop, validate, and document datasets, tables, listings, and figures related to the devices being studied.
• Ability to communicate technical concepts to others.
• In collaboration with data management, may provide specialty SAS programming for data management including customized line listings to support review of clinical trial data.
• Provides programming specifications and directions to the study team/statistical programmers.
• Supports the regulatory review and provide data information for the experimental therapies.
• Ensures that study documentation is maintained to the standard required according to SOPs and acceptable for audit.

Must Have (Minimum Requirements):

To be considered for this role, please ensure the minimum requirements are evident in your applicant profile.

• Bachelor’s degree required
• Minimum of 4 years of statistical programming experience in clinical trial data analysis within the healthcare industry
• Or advanced degree with a minimum of 2 years of statistical programming experience in clinical trial data analysis within the healthcare industry.

Nice to Have (Preferred Qualifications):

• Master’s degree in Biostatistics, Computer Science, or related field