Supply chain lead

870050

CRC Salario confidencial

Costa Rica Alajuela / Otras

Publicado 3 Sep 2025

Salud: médicos

1 Vacante

Asepsa
Industria de la empresa:
Financiero

Descripción general

About the Role
We are seeking a  Clinical Strategy and Management Lead to drive the strategic planning and operational execution of investigational product supply for global clinical trials (Phases I–IV). This role is essential in ensuring timely, compliant, and efficient delivery of clinical supplies across a dynamic and collaborative environment. 
Key Responsibilities
Lead the development and execution of global clinical supply chain strategies aligned with study protocols and milestones.
Act as the primary point of contact for supply planning and execution, collaborating with cross-functional teams and external partners.
Anticipate changes in study design and proactively adjust supply strategies.
Identify and mitigate supply chain risks; develop and implement contingency plans.
Manage clinical trial supply budgets and communicate forecasts; maintain accurate data in tracking systems.
Ensure compliance with regulatory and quality standards; represent supply in audits and inspections.
Support continuous improvement initiatives and collaborate across global time zones.

Requisitos para aplicar

Basic Qualifications
Bachelor’s degree with 5+ years of relevant experience; or master’s degree with 3+ years of relevant experience (or equivalent combination of education and experience).
Background in pharmaceutical or biotech, supply chain, life sciences, health science, project management, or business administration.
Strong understanding of pharmaceutical quality and regulatory frameworks and clinical development.
Proven leadership in matrix environments and cross-functional teams.
Excellent communication skills in English (written and verbal).
Proficiency in Microsoft Office tools, including MS Project and Office Timeline-Pro.
Preferred Qualifications
Knowledge of Good Manufacture Practice (GMP), Good Clinical Practice (GCP), and clinical logistics (e.g., randomization, packaging, labeling, distribution).
Experience managing complex clinical development programs and multiple clinical studies.
Strong skills in budgeting, forecasting, stakeholder alignment, and performance tracking.
Experience presenting in large forums or conferences.

Datos complementarios

870050

Coordinador supervisor o especialista

Enfermero / Otras

Industrias Médicas

5 años de experiencia

Contrato Definido

870050

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