Senior Program Manager, Drug Development & Regulation

Cintrifuse; Cincinnati (OH); On-site; USD 120,000 - 150,000; Full time

Job summary

Cintrifuse is seeking a Senior Program Manager to lead drug partner programs from inception through commercial launch. The candidate will manage product development processes and ensure compliance with healthcare regulations.

The ideal candidate has over 8 years of experience in a regulated industry, with at least 5 years in medical devices or pharmaceuticals, and is skilled in cross-functional team leadership.

Qualifications

• Minimum 8 years of experience in a regulated industry, preferably 5 years in medical devices, pharmaceuticals, or combination products.
• Minimum 3 years of experience leading cross-functional, matrixed teams.
• Experience managing resources, budget, milestones, and detailed activities for large-scale projects.

Responsibilities

• Manage drug partner program(s) from inception through commercial launch.
• Support all phases of the product development process from Concept to Launch.
• Develop, maintain, and nurture positive relationships with stakeholders.

Skills

Leads cross-functional teams

Effective communication skills

Problem solving

Attention to detail

Influences without direct authority

Education

Bachelor of Science in Engineering or Life Science

MBA or Master's in Engineering/Life Science

Tools

Microsoft Office suite

Job description

Cintrifuse is seeking a Senior Program Manager to lead drug partner programs from inception through commercial launch. The candidate will manage product development processes and ensure compliance with healthcare regulations.

The ideal candidate has over 8 years of experience in a regulated industry, with at least 5 years in medical devices or pharmaceuticals, and is skilled in cross-functional team leadership.