Clinical Trials Supply Business Development Lead

Globyz Biopharma Services; Buffalo (NY); On-site; USD 90,000 - 140,000; Full time

Job summary

Globyz Biopharma Services seeks a seasoned sourcing professional to drive new business for Clinical Trials Materials and Comparators. You will lead supply planning, forecast budgets, and coordinate with internal teams and external vendors to ensure timely, compliant CTM delivery across trials.

Key responsibilities include overseeing CTM manufacturing requests at GMP facilities, managing inventory, and ensuring regulatory compliance with FDA/ICH/GMP standards.

Qualifications

• Minimum of 5 years life sciences experience, including labeling, packaging and distribution of clinical trial materials.
• Experience managing labeling, packaging and distribution of materials to clinical sites.
• Knowledge of FDA, ICH, GMP, and other regulatory requirements.
• Demonstrated understanding of pharmaceutical processes, packaging operations and drug development.
• Familiarity with IND/NDA requirements and ability to present complex issues clearly.

Responsibilities

• New Business Development for Clinical Trials Material/Comparators.
• Lead development of Clinical Supply Demand Gathering and Supply Plans.
• Communicate clinical trial requirements to internal stakeholders and external partners.
• Manage vendor relationships where required.
• Oversee manufacture requests for CTM at GMP packaging facility and manage trial inventory.

Skills

Life sciences experience

Project management

Multi-disciplinary teamwork

Stakeholder communication

Tools

MS Office Suite

Word

Excel

PowerPoint

Windows

Job description

Globyz Biopharma Services seeks a seasoned sourcing professional to drive new business for Clinical Trials Materials and Comparators. You will lead supply planning, forecast budgets, and coordinate with internal teams and external vendors to ensure timely, compliant CTM delivery across trials.

Key responsibilities include overseeing CTM manufacturing requests at GMP facilities, managing inventory, and ensuring regulatory compliance with FDA/ICH/GMP standards.