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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in developing and executing clinical supply strategies for Phase I–III studies, with a strong focus on regulatory compliance, inventory optimization, and vendor engagement. Proficient in managing drug supply logistics and documentation while ensuring effective collaboration across cross-functional teams.
Highest-signal resume keywords
Clinical Supply Strategy DevelopmentRegulatory Requirements KnowledgeTrial Management Software ExperienceImport/Export Regulations ExpertiseAdvanced MS Office Proficiency
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Supply ManagementDemand ForecastingRisk AssessmentInventory OptimizationLabel Text DevelopmentDocumentation ManagementDepot ManagementAnalytical SkillsDecision-Making SkillsContinuous Improvement Mindset
Soft Skills
Excellent Communication SkillsStrong Interpersonal SkillsAttention to DetailOrganizational SkillsFlexibility and Adaptability
Tools & Technologies
Trial Management SoftwareMS Office Suite
Industry Keywords
Clinical TrialsPharmaceuticalsGlobal StudiesRegulatory ComplianceSupply Chain Management
About the role
Key responsibilities & impact- Develop and execute end-to-end clinical supply strategies for Phase I–III clinical studies
- Create demand forecasts and supply plans based on study protocols, enrollment assumptions, and country-specific requirements
- Determine proper use of materials as required by governing regulatory agencies
- Perform risk assessments and mitigation planning
- Optimize inventory and minimize waste
- Manage packaging, labeling, distribution, returns, and destruction activities
- Manage label text development
- Coordinate global supply distribution
- Monitor inventory levels
- Ensure clinical trial materials have proper and complete documentation and correct and up-to-date information
- Support vendor engagement activities, including contracts, meetings, invoices, and deliverables
- Collaborate with Clinical Operations, Regulatory Affairs, Quality, and Pharmaceutical Development and Operations teams
- Perform other duties as assigned
Requirements
What you’ll need- Bachelor’s degree in natural sciences, or related field; or relevant experience
- 5+ years of experience in managing drug supply for global studies, or a related area
- Knowledge of regulatory requirements with respect to clinical trial supplies
- Excellent written and verbal communication skills, with ability to influence and build credibility at all levels
- Strong interpersonal skills for interacting with employees and leaders across various levels and functions
- Attention to detail and ability to manage multiple processes and documentation requirements
- Strong technical and analytical skills with advanced knowledge in MS Office including Word, Excel, and PowerPoint
- Experience with trial management software for randomization/supply required
- Proficiency in depot management supporting shipments to sites
- Expert knowledge of import/export regulations and requirements as it pertains to finished pharmaceuticals
- Knowledge of tariffs, duties and VAT requirements, as appropriate
- Ability to work in a team or independently as required
- Outstanding organizational skills with the ability to prioritize
- Demonstrated independent and sound decision-making skills; ability to think critically and make decisions in a fast-paced environment
- Continuous improvement mindset; seeking ways to drive innovation and efficiencies throughout the organization
- Flexible and willing to learn; adapting to business and site needs in a dynamic environment
- Maintain a positive, approachable and professional attitude
Benefits
Comp & perks- Annual performance incentive bonus
- New hire equity package
- Medical insurance
- Dental insurance
- Vision insurance
- 401(k) match
- PTO
- Paid holidays
