Cell Therapy Launch Director, Northeast

Pierre Fabre; United States; Remote; USD 170,000 - 250,000; Full time

Benefits offered by this job

Medical, dental, and vision coverage

401(k) retirement plan

PTO and paid holidays

Paid parental leave

Employee discounts on products

Professional development opportunities

Mental health and wellness programs

Job summary

Pierre Fabre is building a new US division focused on rare diseases and oncology, seeking a Cellular Therapy Director to guide the launch of Tab-cel. You will drive disease awareness, build expert networks, and onboard treatment centers, delivering patient-centric, innovative solutions while scaling the US presence.

The role requires deep CGT expertise, strong leadership, and cross-functional collaboration to navigate pre- and post-approval activities and to expand access for eligible patients

Qualifications

• Bachelor’s Degree required.
• At least 10 years of experience in biopharma.
• Deep expertise in cell or gene therapy service lines.
• Experience in a collaborative matrix environment.
• Ability to convey complex treatment modalities clearly.
• Sales experience in ultra-rare disease or CGT.

Responsibilities

• Lead disease awareness efforts for Tab-cel in the pre-approval phase.
• Develop relationships with clinical and non-clinical experts to understand unmet needs.
• Onboard sites for launching allogeneic cell therapy.
• Drive demand and support utilization post-approval across institutions.
• Coordinate cross-functionally with medical, value & access, and operations teams.
• Map accounts and pharmacist/physician workflows to enable access.

Skills

Biopharma sales

Rare diseases

Cell therapy CGT

Matrix collaboration

Scientific aptitude

Education

Bachelor’s degree

Job description

Pierre Fabre is building a new US division focused on rare diseases and oncology, seeking a Cellular Therapy Director to guide the launch of Tab-cel. You will drive disease awareness, build expert networks, and onboard treatment centers, delivering patient-centric, innovative solutions while scaling the US presence.

The role requires deep CGT expertise, strong leadership, and cross-functional collaboration to navigate pre- and post-approval activities and to expand access for eligible patients