Director/Senior Director Program Managment

Barrington James; United States; Remote; USD 100,000 - 125,000; Full time

Job summary

An exciting opportunity awaits with a forward-thinking pharmaceutical company seeking a Head of Program Management. This pivotal role focuses on leading program execution and strategic operations for a solid oral program in phase 2, driving success towards NDA submission and commercialization. The ideal candidate will thrive in a dynamic environment, collaborating with C-suite executives and external partners to ensure alignment and progress. If you are a hands-on leader with a proven track record in the biotech industry, this position offers the chance to make a significant impact in a growing company. Join a team that values innovation and excellence in the pharmaceutical field.

Qualifications

• Proven track record in NDA submissions and product launches in biotech/pharma.
• Hands-on leader with experience in small molecule product development.

Responsibilities

• Lead program strategy and execution for NDA submission and approval.
• Oversee timelines, budgets, and operational strategy for regulatory success.

Skills

NDA submissions

Product launches

Program management

Cross-functional collaboration

Risk management

Small molecule product development

Adaptability

Education

Degree in a scientific field

MBA

Tools

PMP certification

Job description

Director/Senior Director Program Management

Head of Program Management (Director/Snr Director) - Remote

I am currently collaborating with an exciting up-and-coming Pharma who are seeking a Head of Program & Operations to lead program management and strategic operations to help with the development of their lead solid oral program, currently sitting in phase 2.

As the company prepares for its NDA submission and commercialization, this role will be essential in driving program execution, ensuring cross-functional alignment, and managing key external partnerships. The ideal candidate is a hands-on leader with proven experience in NDA approvals and product launches, capable of working closely with executive leadership, internal teams, and external stakeholders to drive success in a dynamic, fast-paced environment.

Key Responsibilities:

• Lead program strategy and execution, ensuring seamless progress toward NDA submission and approval.
• Work cross-functionally with C-suite executives, internal teams, and external partners to align on objectives and timelines.
• Oversee program timelines, budgets, risk management, and operational strategy to support regulatory and commercial success.
• Provide strategic oversight of product development and lifecycle management, ensuring readiness for launch.
• Act as a key liaison between internal teams and external vendors, including CDMOs, CROs, and regulatory agencies.
• Foster a collaborative and high-performance culture, taking a proactive, hands-on approach to challenges.

Qualifications & Experience:

• Degree in a scientific field and MBA preferred but not essential.
• Proven track record of working with NDA submissions/launches and gaining approvals in the biotech/pharma industry.
• PMP certification preferred but not essential.
• Strong background in small molecule product development and commercialization.
• Experience in solid oral preferred but not essential.
• Experience working directly with executive leadership and external partners in a small, dynamic team environment.
• Hands-on, adaptable, and proactive—comfortable taking initiative and managing multiple priorities.
• Ability to navigate a fast-paced, growing biotech company, driving execution with limited resources.

Apply today to learn more or reach out directly to [e-mail]

Seniority Level

Director

Employment Type

Full-time

Job Function

Strategy/Planning and Project Management

Industries

Pharmaceutical Manufacturing