Global Oncology Regulatory Program Lead

Medasource; New Jersey; On-site; USD 100,000 - 130,000; Full time

Job summary

A leading healthcare consulting firm is seeking a Regulatory Program Manager in New Jersey. This role involves driving global regulatory strategy into executable plans and coordinating cross-functional teams. The ideal candidate will have significant operational leadership experience, familiarity with regulatory submissions, and a strong background in project management. Required qualifications include a Bachelor's degree and proficiency in MS Project, with at least 5 years in relevant industry experience., Providing strategic oversight to ensure the success of the Oncology portfolio is essential.

Qualifications

• Minimum of 5 years of industry/business experience required.
• Minimum of 3 years in Pharmaceutical, MedTech or comparable R&D area required.
• Experience in strategic planning and development of global regulatory strategy required.

Responsibilities

• Drive projects through translation of global regulatory strategy.
• Empower teams to deliver impact for programs and patients.
• Ensure alignment of functional plans with compound objectives.

Skills

Project management

Strategic planning

Regulatory knowledge

Communication

Innovative thinking

Education

Bachelor’s degree in Life Sciences or related field

Tools

MS Project

Job description

A leading healthcare consulting firm is seeking a Regulatory Program Manager in New Jersey. This role involves driving global regulatory strategy into executable plans and coordinating cross-functional teams. The ideal candidate will have significant operational leadership experience, familiarity with regulatory submissions, and a strong background in project management. Required qualifications include a Bachelor's degree and proficiency in MS Project, with at least 5 years in relevant industry experience., Providing strategic oversight to ensure the success of the Oncology portfolio is essential.