Sr. Associate, Clinical Supplies Planning and Logistics

Structure Therapeutics; United States; Sur place; USD 52 000 - 78 000; Plein temps

Résumé du poste

Scorpion Therapeutics seeks an entry-level Clinical Supplies Professional to support clinical trial logistics in a biotech environment. You will participate in demand forecasting, packaging, labeling, inventory management, and distribution coordination for multiple trials.

Collaborate with CROs, CMOs, IRT, clinical operations, regulatory, and QA to ensure compliance and smooth execution, documentation, batch record review, and inspection readiness.

Qualifications

• BA/BS in a scientific discipline or supply chain.
• 3+ years in clinical supplies, QA, manufacturing, or related GxP environments.
• Knowledge of cGMP, GCP, GDP.
• Strong Excel/Office skills.
• Ability to manage multiple priorities and collaborate across global teams.

Responsabilités

• Participate in demand forecasting, packaging, labeling, inventory management, and distribution coordination for multiple trials.
• Collaborate with external vendors (CROs, CMOs, IRT), clinical operations, regulatory, and QA teams to ensure compliance and smooth execution.
• Assist in documentation, batch record review, and inspection readiness.

Connaissances

Excel

Office suite

Cross-functional collaboration

Global collaboration

Formation

BA/BS in science or supply chain

Description du poste

Role: Entry-level Clinical Supplies Professional supporting clinical trial logistics within a biotech-focused environment.

Responsibilities

• participate in demand forecasting, packaging, labeling, inventory management, and distribution coordination for multiple trials
• collaborate with external vendors (CROs, CMOs, IRT), clinical operations, regulatory, and QA teams to ensure compliance and smooth execution
• assist in documentation, batch record review, and inspection readiness

Requirements

• BA/BS, preferably in a scientific discipline or supply chain
• 3+ years in clinical supplies, QA, manufacturing, or related GxP environments
• knowledge of cGMP, GCP, GDP
• strong Excel/Office skills
• ability to manage multiple priorities and collaborate across global teams

Preferred

• experience in global logistics
• GxP compliance
• familiarity with regulatory documentation

HighValue

• clinical supply chain management in biotech, GxP environment, supporting clinical trials (phases not specified), interaction with vendors and study teams
• travel up to 10%

WorkSetup

predominantly remote with some travel.