Veristat
Website:
veristat.com
Job details:
Job Description
Senior Manager, Statistical Programming
The Senior Manager, Statistical Programming is responsible for the statistical programming aspects of projects for clients and project teams through management of internal staff. Working closely with the Director, Statistical Programming, s/he maintains optimal department processes, implements project-specific strategies, and assists with the development and implementation of department strategies to increase productivity and quality, while decreasing cycle times and costs.
Make an Impact at Veristat!
Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.
- 105+ approved therapies for marketing applications prepared by Veristat
- 480+ oncology projects in the past 5 years
- 350+ rare disease projects delivered in the past 5 years
- Flexible, inclusive culture — 70% remote workforce, 66% women-led teams
- Learn more about our core values here!
What We Look For
- Master’s degree in technology, statistics, pharmaceutics or another related science, mathematics, or engineering field, with a minimum of 5 years of SAS programming experience with clinical trial data using CDISC SDTM and ADaM implementation guidelines OR Bachelor’s with a minimum of 8 years of SAS programming experience with clinical trial data using CDISC SDTM and ADaM implementation guidelines.
- 3 years of supervisory experience, preferably in a CRO environment; therein, demonstrated ability to successfully lead a team of programmers.
- Excellent working knowledge of CDISC SDTM and ADaM Implementation Guidelines.
- Advanced skills in SAS and other statistical applications, and ability to learn new applications required.
- Demonstrated ability to think “big picture” and strategically leverage expertise, to serve as a consultant and business partner with internal and external customers.
- Demonstrated ability to thoughtfully solve problems, exercise sound judgment, lead by example, and influence without authority.
- Thorough knowledge of International Conference on Harmonisation (ICH) Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines as well as of medical terminology, clinical trials, and clinical research.
- Working knowledge of the relationship and regulatory obligation of the contract research organization (CRO) industry with pharmaceutical and biotech companies.
- Excellent knowledge of regulatory requirements and drug development process.
- Excellent interpersonal, communication, and organizational skills with the ability to work independently and in a fast paced, team environment.
Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.
Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Click on Apply to know more.