FSP - Sr Regulatory Program Manager - client dedicated

Ladders; United States; Remote; USD 120,000 - 145,000; Full time

Benefits offered by this job

Standard Monday to Friday workweek

Office‑based work environment

Job summary

Ladders is seeking a Sr Regulatory Program Manager to lead regulatory program execution for client-dedicated work in the Pharmaceuticals & Biotech space. You will translate global regulatory strategy into actionable plans with milestones, risks, and accountability in a matrix environment. Location: Remote - US based candidates only.

Compensation: $120,000 – $145,000 annually. You will partner with regulatory leadership and cross-functional teams to keep submissions on track across international

Qualifications

• Bachelor level degree in a scientific, engineering or healthcare field.
• Advanced degree (MS/PhD/PharmD) preferred; PMP cert is a plus.
• Regulatory program management experience sought.

Responsibilities

• Partner with global regulatory leads to develop and execute regulatory plans.
• Translate regulatory strategies into actionable plans with milestones and risks.
• Lead execution of regulatory plans aligning with strategic objectives.
• Identify innovative regulatory pathways meeting global expectations.
• Collaborate with cross-functional teams to ensure accountability for deliverables.
• Facilitate global regulatory subteam meetings with structured agendas and decisions.
• Apply project management to improve meetings and documentation.

Skills

Regulatory program leadership

Cross-functional collaboration

Regulatory strategy translation

Communication

Education

BA/BS in science/engineering/healthcare

MS/PhD or PharmD preferred

PMP certification preferred

Tools

eCTD experience

IND/BLA/MAA submissions

Job description

For our client, we are seeking a Sr Regulatory Program Manager to join the team of a leader in the Pharmaceuticals & Biotech space.

This role will drive regulatory program execution for client-dedicated work, helping translate global regulatory strategy into clear plans, milestones, and risk management actions. You will partner closely with regulatory leadership and cross-functional teams to coordinate deliverables, improve subteam meeting effectiveness, and keep complex submissions on track across international markets. The position requires strong program leadership, regulatory fluency, and the ability to bring structure and accountability to a matrixed environment.

Location: Remote - US based candidates only, no visa sponsorship available

Compensation: $120,000 – $145,000 annually

Responsibilities

• Partner with global regulatory leads to develop and execute regulatory plans
• Translate regulatory strategies into actionable plans with clear milestones and risks
• Lead execution of regulatory plans, aligning operations with strategic objectives
• Identify innovative regulatory pathways that meet global expectations
• Collaborate with cross-functional teams to ensure accountability for regulatory deliverables
• Facilitate effective global regulatory subteam meetings with structured agendas and a decision‑making focus
• Apply project management best practices to enhance meeting effectiveness and documentation

Qualifications

• BA/BS in a scientific, engineering, or healthcare discipline; advanced degree (MS, PharmD, PhD) and/or PMP certification preferred
• 7+ years in pharmaceutical, biotechnology, or life sciences, with 5+ years in regulatory or program management
• Experience with IND/BLA/MAA submissions and global registration processes
• Strong understanding of U.S. regulatory requirements and international regulations
• Proven ability to manage complex regulatory deliverables in a matrixed organization
• Hands‑on experience with eCTD and regulatory documentation
• Exceptional communication skills for synthesizing complex information

Benefits

• Standard Monday to Friday work schedule
• Office‑based work environment

Our client is an equal opportunity employer.