Senior Manager, Clinical Supply Integration

Olema Oncology; Cambridge (MA); On-site; USD 150,000 - 190,000; Full time

Job summary

Scorpion Therapeutics is seeking a Senior Manager, Clinical Supply Integration to oversee end-to-end management of investigational medicinal products (IMPs) for global oncology trials. You will coordinate supply activities across manufacturing, packaging, labeling and distribution, manage timelines, dependencies and risks, and collaborate with Clinical Operations, CMC, Quality, Regulatory, and Finance.

Based in San Francisco or Boston with 10-15% travel, this role drives process improvements and

Qualifications

• Bachelor’s degree (Master’s preferred) with 8+ years in clinical supply for biotech/pharma.
• Deep knowledge of GMP, GDP, regulatory standards and clinical supply processes.
• Experience supporting late-stage global studies and vendor management.
• Strong project and cross-functional leadership in a matrix organization.

Responsibilities

• Coordinate supply activities across manufacturing, packaging, labeling, and distribution vendors.
• Manage logistics, timelines, dependencies, and risks.
• Collaborate with Clinical Operations, CMC, Quality, Regulatory, and Finance teams.
• Maintain supply documentation and budgets; drive improvements and SOP development.

Skills

Clinical supply

Vendor management

Logistics planning

Regulatory compliance

Education

Bachelor's degree

Master's degree preferred

Tools

Clinical ERP systems

Regulatory databases

Job description

Role

Senior Manager, Clinical Supply Integration, overseeing end-to-end management of investigational medicinal products (IMPs) to ensure timely and compliant delivery for global oncology clinical trials.

Responsibilities

coordinate supply activities across manufacturing, packaging, labeling, and distribution vendors; manage logistics, timelines, dependencies, and risks; collaborate with Clinical Operations, CMC, Quality, Regulatory, and Finance teams; maintain supply documentation and budgets; drive process improvements and SOP development.

Requirements

Bachelor's degree (Master's preferred), 8+ years in clinical supply within biotech/pharma, with experience supporting complex, late-stage global studies; deep understanding of GMP, GDP, regulatory standards, and clinical supply systems; vendor management expertise.

Preferred

oncology trial experience, familiarity with inventory, demand planning, and logistics.

High-Value

global clinical supply chain, late-stage (Phase 3) oncology trials, regulatory compliance, cross-functional collaboration, project management skills, and operational excellence.

Work setup

based in San Francisco or Boston, with 10-15% travel.