Remote Associate Director, Pharmaceutical Development

Ladders; United States; On-site; USD 223,000 - 239,000; Full time

Benefits offered by this job

Annual bonus

Company equity

Employer-paid health premiums

401(k) matching

Remote work with travel

Job summary

Ladders seeks an Associate Director/Director of Pharmaceutical Development to lead strategic CMC guidance and robust formulation programs. This remote US-based role partners with field leadership and cross-functional teams to drive scalable processes, ensure safety, quality, and execution discipline across development programs.

You will oversee CRO activities, manage drug forecasts, and support regulatory submissions to improve operational performance and customer outcomes within a life sciences

Qualifications

• PhD or advanced degree in Chemistry or Pharmacy.
• 7+ years of experience in the bio/pharmaceutical industry focused on formulation development and Clinical Supply.
• Expertise in formulation with knowledge of PK/PD principles and ADME concepts.
• Experience with regulatory documentation and authorship.
• Demonstrated ability to manage Clinical Supply and formulation at CROs.

Responsibilities

• Provide strategic CMC guidance to cross-functional project teams.
• Develop robust formulations and manufacturing processes for QED products.
• Review and ensure compliance of development and manufacturing programs at CROs.
• Manage drug forecasts and associated transactions.
• Support regulatory submission preparation with formulation and clinical supply expertise.

Skills

Formulation development

Clinical Supply management

Regulatory documentation

Cross-functional leadership

Project management

Education

PhD or advanced degree in Chemistry or Pharmacy

Job description

Ladders seeks an Associate Director/Director of Pharmaceutical Development to lead strategic CMC guidance and robust formulation programs. This remote US-based role partners with field leadership and cross-functional teams to drive scalable processes, ensure safety, quality, and execution discipline across development programs.

You will oversee CRO activities, manage drug forecasts, and support regulatory submissions to improve operational performance and customer outcomes within a life sciences