Global Clinical Supply Chain Manager

Scorpion Therapeutics; United States; On-site; USD 124,000 - 176,000; Full time

Benefits offered by this job

Discretionary bonus

Long‑term incentives

Paid time off

Medical insurance

Dental insurance

Vision insurance

Life insurance

Job summary

Scorpion Therapeutics seeks a Clinical Supply Manager to translate study protocols into demand, supply planning and depot inventory for global trials. You will forecast 9–18 months and convert forecasts into CPL plans, coordinating with logistics and QA to ensure compliant, on‑time shipments.

The role requires a Bachelor’s (or Master’s) with experience in clinical supply, SAP/IVRS/QMS, and cross‑functional collaboration across regions.

Qualifications

• Bachelor's degree (or Master’s) with relevant clinical supply experience.
• Experience in forecasting, demand/supply planning and distribution strategies.
• Knowledge of GMP/GDP and global shipping regulations.

Responsibilities

• Translate clinical study protocols into IMP demand, supply planning and depot inventory.
• Forecast and plan 9–18 months; convert forecasts to CPL execution plans.
• Review contracts/quotes; process POs and reconcile invoices.
• Develop depot/site seeding and resupply strategies; ensure on‑time shipments.
• Collaborate across functions to resolve shipping issues and drive CAPAs.
• Support regulatory filings/inspections and maintain CSR/TMF compliance.
• Use SAP/IVRS/QMS to progress IMP and author SOPs.

Skills

Forecasting

Demand planning

Supply planning

Logistics coordination

Cross-functional collaboration

Regulatory compliance

Education

Bachelor’s degree

Master’s degree

Tools

SAP

IVRS

QMS

Job description

Job Responsibilities:

• Interpret clinical study protocols/dosing schemas and translate into IMP demand/supply planning, distribution strategies, and depot inventory management.


• Perform demand and/or supply forecasting and planning (9–18 months).


• Translate forecasts into clinical packaging and labeling (CPL) execution plans.


• Support contract/quote reviews; purchase order and invoice reconciliations.


• Develop and implement depot and clinical site seeding and resupply strategies.


• Execute logistics/operational strategies with Quality Assurance and other groups to ensure on‑time, safe delivery of clinical shipments.


• Collaborate with Logistics, GCSC, PDM, and partners to resolve shipping issues; escalated as needed.


• Support clinical development and PDM strategies to deliver compliant, quality IMP globally on time in full.


• Ensure accurate depot inventory/records; track incidents and resolve root causes; assist with CAPAs.


• Use systems (e.g., SAP, IVRS, QMS) to progress IMP; author SOPs/business process work instructions.


• Support regulatory filings/inspections; maintain CSR and TMF compliance.


• Maintain GDP/GMP and global trade compliance; keep training compliant.


• Obtain/review quotes; approve purchase requisitions and invoices.

Basic Qualifications:

• Bachelor’s + 6 years’ experience; OR Master’s + 4 years’ experience.

Preferred Qualifications:

• Clinical supply management expertise (forecasting, demand/supply planning, distribution strategies, IVRS/ERP).


• Clinical study design/blinding/global trials knowledge (Phase 1–late); CD&OP knowledge.


• Experience managing comparator drugs/co-meds.


• Ability to collaborate/influence/negotiation with cross-functional teams and suppliers.


• Communication, computer skills, and ability to manage complex study/program timelines (PM experience a plus).

People Leader Accountabilities:

• Create Inclusion; Develop Talent; Empower Teams.

Compensation/Benefits (as stated):

• Bay Area: $136,340–$176,440; Other US: $123,930–$160,380. Discretionary bonus/long-term incentives, paid time off, and company-sponsored medical/dental/vision/life insurance.