Manager, Program Excellence – (IS, MRC) at Novartis
Insurgentes, QRoo., Mexico -
Full Time


Start Date

Immediate

Expiry Date

27 Sep, 25

Salary

0.0

Posted On

28 Jun, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

C2, Business Meetings, Teams, Global Experience

Industry

Information Technology/IT

Description

SUMMARY

TThe Manager, Program Excellence Supports the Director, Evidence Generation Program Excellence in the management and prioritization of USMA departmental applications/functions. Responsible for department level activities as assigned with a tactical approach, which requires the ability to multi-task on a wide spectrum of activities with an overall clinical trial operational focus.

ESSENTIAL REQUIREMENTS:

  • Advanced English, level C1 – C2
  • Candidate must have 5 years project management, technical, and operational experience and 3 years working directly in clinical trial execution with country and/or global experience.
  • Bachelor’s degree in scientific or healthcare discipline is preferred, (preference for sciences).
  • Experience with running and managing critical business meetings with multiple cross functional stakeholders.
  • Experience with Pleasereview is recommended.
  • Proven ability to work independently and ability to collaborate and work effectively in teams. Demonstrated ability to support multiple projects.
Responsibilities

ABOUT THE ROLE

This role is based in Mexico City, Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

KEY RESPONSIBILITIES:

  • Manage and execute the medical review of all concepts/project plans, and protocols for the US-MA organization.
  • Support the development, update and presentation of training materials related to clinical trial process.
  • Assist with the oversight of revising/implementation of trial submission processes. This includes but not limited to QC of all concept submissions, workflow tracking across review process, tracking milestones from submission to final approval/rejection.
  • Work with clinical teams and information technology to identify, prioritize and resolve issues. This includes being the first line support and providing timely response of questions and required reports.
  • Aid the implementation of innovative, transformative and sustainable solutions to accelerate data generation activities. Understand trial prioritization and be able to assist teams with questions related to prioritization.
  • Work with the Director, Evidence Generation Program Excellence to help project teams define and provide clarity on business process and business requirements for prioritization and metrics tracking.
  • Supports the development of the project plan for annual prioritization activities including open research questions (ORQs).
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