Lead Statistical Programming Manager – Medical Devices

Penumbra, Inc.; Home (KS); On-site; USD 158,000 - 227,000; Full time

Job summary

Penumbra, Inc. is seeking a Manager of Statistical Programming to lead a team of statisticians and programmers supporting medical device clinical research, regulatory submissions, and publications.

You will shape programming standards, mentor staff, oversee SAPs and datasets, collaborate across Regulatory, Data Management, Scientific Communications, and Clinical Study Management, and ensure timely, compliant deliverables.

Qualifications

• Bachelor’s degree in Statistics, Data Science, Computer Science, Mathematics, or related field with 8+ years of experience or equivalent combination of education and experience.
• In-depth knowledge of statistical programming concepts and techniques related to medical devices or drug development is required.

Responsibilities

• Lead a team of statistical programmers. Develop and oversee the development of statistical code for Tables, Listings and Figures for clinical studies.
• Oversee resource planning for statistical programming team, including forecasting of employees and external resources.
• Monitor and quantify efficiency, accuracy, and timeliness of the group.
• Mentor others on existing Macros and oversee development of new SAS Macros.
• Manage CROs and outside vendors for statistical programming activities.

Skills

Staff management

Leadership

Statistical programming

SAS macros

Regulatory knowledge

Cross-functional collaboration

Project estimation

Mentoring

Education

Bachelor's degree in Statistics/CS/Math

8+ years experience

Tools

SAS

R

Python

Git

Job description

Penumbra, Inc. is seeking a Manager of Statistical Programming to lead a team of statisticians and programmers supporting medical device clinical research, regulatory submissions, and publications.

You will shape programming standards, mentor staff, oversee SAPs and datasets, collaborate across Regulatory, Data Management, Scientific Communications, and Clinical Study Management, and ensure timely, compliant deliverables.