Director, Medical Information

CG Oncology, Inc.

United States

On-site

USD 180,000 - 260,000

Full time

14 days+

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Job summary

CG Oncology is seeking a Director of Medical Information to oversee the development and management of Medical Information functions for bladder cancer immunotherapies. The role focuses on scalable content, regulatory compliance, and cross-functional collaboration to support product launches and lifecycle management.

The position emphasizes leadership in program development, content management, and digital solutions, with the team operating fully remotely within the United States.

Qualifications

  • Advanced degree and 10+ years in pharma/biotech with 4–5 years in Medical Information.
  • Proven leadership in program development and content management.
  • Experience with GxP, regulatory review, and digital solutions.

Responsibilities

  • Create scalable Medical Information content strategies and ensure regulatory compliance.
  • Manage outsourced call center operations and analyze inquiry metrics.
  • Lead digital transformation initiatives and collaborate with Medical Affairs, Clinical Development, Market Access, and Regulatory teams.
  • Support scientific activities at congresses.

Skills

Leadership
Strategic thinking
Cross-functional collaboration
Regulatory knowledge

Education

Advanced degree (PharmD, PhD, MD)

Tools

GxP systems
Regulatory review
Digital solutions

Job description

Role

Director of Medical Information at CG Oncology, overseeing development and management of Medical Information functions to support product launches, lifecycle management, and stakeholder engagement in bladder cancer immunotherapies.

Responsibilities

Responsibilities include creating scalable content strategies, ensuring regulatory compliance, managing outsourced call center operations, analyzing inquiry metrics, and leading digital transformation initiatives. The role involves cross-functional collaboration with Medical Affairs, Clinical Development, Market Access, and Regulatory teams, and supporting scientific activities at congresses.

Qualifications

Advanced degree (PharmD, PhD, MD), 10+ years in pharma or biotech with 4-5 years in Medical Information, proven leadership in program development and content management, and experience with GxP, regulatory review, and digital solutions.

Preferred skills

Vendor management, analytical capabilities, and experience supporting late-stage development or product launches.

High-Value

Focus on immunotherapies for bladder cancer, compliance with medical information standards, development of scientific content, and implementation of innovative tech solutions.

Work setup

Fully remote in the U.S., with no travel specified.

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