Sr. Associate Global Study Planner | BREDA

Senior Associate Global Study Planner
Pharmaceutical / Biotechnology

Job Description
The Senior Associate Global Study Planner independently manages demand and supply planning for clinical studies with a global scope. This includes ensuring adequate finished drug product supplies from study initiation through closure, coordinating operational inventory management, and minimizing waste. The role involves cross-functional collaboration, performance tracking, and adherence to supply chain processes and regulatory guidelines.

Non-Negotiable Skills, Qualifications, and Experience

• Bachelor’s degree or equivalent in logistics, business administration, or related field.

• Minimum 5 years of relevant experience in supply planning.

• Experience in supply planning within the pharmaceutical industry.

• Fluency in English (verbal and written).

Essential Skills, Qualifications, and Experience

• Knowledge of clinical supply chain management.

• Experience in forecasting drug demand and managing inventory for clinical studies.

• Ability to coordinate packaging, labeling, and shipment of clinical supplies.

• Experience using ERP systems, preferably SAP.

• Proficiency in MS Office applications.

• Understanding of regulatory guidelines impacting clinical supplies.

• Ability to identify and escalate risks to study timelines or clinical supply availability.

• Experience participating in cross-functional planning meetings and stakeholder communications.

• Familiarity with dashboards and internal systems to track supply chain performance.

Desirable Skills, Qualifications, and Experience

• Advanced experience in MS Office applications beyond basic proficiency.

• Experience negotiating resource conflicts in supply chain planning.

• Experience updating or creating procedures per Good Manufacturing Practices (GMP).

• Experience representing planning teams in operational improvement initiatives
  
  Interested? Send an email to f.chauca@panda-int.com or apply now!.