Remote Associate Director, Global Clinical Supply Chain

Ladders; États-Unis; À distance; USD 150 000 - 185 000; Plein temps

Avantages offerts par ce poste

Medical, dental, and vision insurance

Paid time off

Retirement plan options

Access to voluntary benefits

Résumé du poste

Ladders is seeking an Associate Director, Clinical Supply Chain for a remote role, leading global clinical drug supply strategy for late-stage programs. You’ll forecast demand, manage risks, and coordinate with vendors, sites, and cross-functional teams to ensure investigational products are available when needed.

The role emphasizes budget accountability, collaboration with IRT vendors, and ensuring GMP/GCP compliance across trials. This position is fully remote with global impact.

Qualifications

• Bachelor's degree in engineering or a scientific field.
• 12 years of experience in clinical supply and late-stage programs.
• Knowledge of cGxP including GMP, GLP, and GCP.
• Experience managing packaging and labeling CMOs.
• Strong written, verbal, and presentation communication skills.
• Ability to uphold core values in a remote environment.

Responsabilités

• Develop and implement global clinical drug supply strategies.
• Forecast investigational product demand based on study metrics and requirements.
• Manage risks related to drug demand versus production with stakeholders.
• Oversee clinical trial supply management with IRT vendors and systems.
• Contribute to clinical pharmacy manual content and collaborate with clinical sites.
• Manage drug shipment processes and resolve related issues.
• Represent clinical supply on cross-functional study teams while managing budget responsibilities.
• Handle the acquisition and management of comparator drugs.

Connaissances

Strong communication

Remote work culture

Formation

Bachelor's degree in engineering or science

Description du poste

Ladders is seeking an Associate Director, Clinical Supply Chain for a remote role, leading global clinical drug supply strategy for late-stage programs. You’ll forecast demand, manage risks, and coordinate with vendors, sites, and cross-functional teams to ensure investigational products are available when needed.

The role emphasizes budget accountability, collaboration with IRT vendors, and ensuring GMP/GCP compliance across trials. This position is fully remote with global impact.