Jobs and Careers
TA

Senior Manager, Programming

Takeda
United Statesfull_timeVerifiedPosted 3 Feb 2025
💰 $209,000/yr($133,000/yr$209,000/yr)

About the role

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

OBJECTIVES/PURPOSE:

Takeda SQS is looking to add individuals to our team that are team oriented, collaborative, strong understanding of the statistical programming function, exceptional leaders and innovators.  Takeda is a global, values-based, R&D-driven, top 10 biopharmaceutical leader committed to discover and deliver life-transforming treatments, guided by our commitment to patients, our people and the planet.

To attract and retain the very best talent, we in Takeda SQS are open to flexible or remote working for some roles.  Such roles will have a connection to a Takeda R&D center.

ACCOUNTABILITIES:

  • Leads statistical programming activities across multiple studies (or across a compound) and related oversight activities ensuring quality and timeliness

  • Contributes to asset level strategies

  • Independently completes tasks and prioritization

  • Engages cross functionally to progress tasks with proven influencing skills

  • Contributes to and/or leads process improvement initiatives

  • Exhibits existing internal and external presence on topics of interest

CORE ELEMENTS RELATED TO THIS ROLE:

  • Effectively drives and influences project teams towards objectives while enabling and making decisions

  • Combines strong general knowledge of technical and programming methods with applied experience to complete tasks and mentor more junior staff

  • Leads non-project initiatives across statistical programming

  • Demonstrates advanced knowledge of CDISC standards, medical terminology, clinical trial methodologies, and FDA/ICH regulations

  • Leads and organizes programming activities for assigned clinical studies and projects

DIMENSIONS AND ASPECTS:

Technical/Functional (Line) Expertise:

  • Comprehensive understanding of the pharmaceutical industry and statistical programming (e.g., clinical development, the prescription drug distribution process, etc)

  • Excellent analytical, technical, and computer skills

  • Expert level SAS programming ability and experience with other analytical tools, e.g. R, Python.

  • Advanced knowledge of CDISC standards, medical terminology, clinical trial methodologies, and FDA/ICH regulations

Leadership:

  • Demonstrated ability to work and influence across functions, regions and cultures

  • Excellent communicator, able to convey both complex ideas and data, verbally and in writing

  • Proven skills as an effective team player who can engender credibility and confidence within the company

  • Ability to distill complex technical programming ideas in simple comprehensible terms in order to influence decisions and outcomes

  • Embraces and demonstrates a diversity and inclusion mindset

  • Leads projects directly or indirectly related to GPTs or other functions

  • Independently works and prioritizes projects

  • Effectively drives and influences project teams towards objectives while enabling and making decisions

  • Contributes to asset level strategies

  • Has internal and external presence on topics of interest

Decision-making and Autonomy:

  • Recommends strategic decisions that impact the statistical programming function

  • Accountable for statistical programming decision making within study level

  • Participates in initiatives that seek diverse input fro

Apply for this role

Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.

Apply Now →Generate Application Kit

Free account required — sign up in 30s

Company

Takeda

View company profile →