Logo for Elevar Therapeutics

Associate Director, Clinical Supply Chain (Remote)

Role overview

Qualifications

  • Bachelor’s degree in an engineering or scientific field
  • 12 years’ experience in clinical supply, including support of late-stage clinical development programs
  • Knowledge of cGxP (GMP, GLP, GCP etc.), IRT, and relevant quality systems
  • Effective communication skills including written, verbal, and presentation skills

Responsibilities

  • Develop and implement end-to-end clinical drug supply strategies for global clinical studies
  • Forecast investigational product demand based on enrollment, recruitment rates, protocol design, and country-specific requirements
  • Manage risks related to drug demand vs production including working with internal Elevar stakeholders and external partners
  • Work with Interactive Response Technology (IRT) vendors and systems to manage clinical trial supplies and ensure minimal risk to shortage of supplies

Key facts

  • Remote from: United States
  • Full time
  • Expert & Leadership (>10 years)
  • Director of Supply Chain
  • English

Hard skills

Other skills

  • Packaging And Labeling
  • Communication
  • Collaboration
  • Problem Solving
  • Compassion

About the company

Elevar Therapeutics logo

Elevar Therapeutics

Biotechnology

Elevar Therapeutics is a rapidly growing, fully integrated biopharmaceutical company built on the promise of elevating treatment experiences and outcomes for patients who have limited or inadequate therapeutic options. Our experience is rooted in oncology, and we apply the same rigor and diligence that comes with this knowledge to identifying and developing promising medicines for complex yet under-treated health conditions across a range of therapeutic areas.We develop and assess therapeutics based upon their ability to make a meaningful impact for patients and their treatment experiences. We invest in proven and promising therapeutics at various stages of development and advance them through clinical and regulatory processes with the goal of commercializing improved treatment options for patients and the healthcare providers who treat them. Elevating Outcomes: We take a relentless and inventive approach towards developing and advancing next generation, best-in-class therapies that have the potential to set new standards of care and improve treatment experiences.Evolving Therapeutic Potential: We identify areas where we can develop, build upon or evolve medicines that offer patients improved clinical outcomes. Engaging with Purpose: We are committed to engaging with the highest ethical standards, driven by a passion to address the underserved needs of patients, caregivers and healthcare providers.

Company details

Company typeScaleup
IndustryBiotechnology
Company size51 - 200

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Job description

Description

The Associate Director, Clinical Supply Chain is responsible for enabling the timely supply of appropriately packaged and labelled clinical trial material for Elevar. This role will work in conjunction with clinical, regulatory, quality, and CMC teams to ensure all ongoing clinical studies are appropriately supplied. This is a remote-based position located in the United States.

Responsibilities:

  • Develop and implement end-to-end clinical drug supply strategies for global clinical studies
  • Working with clinical, forecast investigational product demand based on enrollment, recruitment rates, protocol design, and country-specific requirements
  • Develop effective plans while managing risks related to drug demand vs production including working with internal Elevar stakeholders and external partners to manage production, expiry, and inventory
  • Work with Interactive Response Technology (IRT) vendors and systems along with relevant stakeholders to manage clinical trial supplies located at manufacturers, depots, and sites while ensuring minimal risk to shortage of supplies
  • Contribute to content of the clinical pharmacy manuals, e.g., shipping, storage, and disposal instructions as well as working directly with clinical sites as requested, to dispose of unused/expired clinical supplies
  • Manage drug shipment requests received from clinical operations and/or clinical sites, including tracking shipments to sites, management of any issues during shipment, responding to any clinical site questions related to drug supply to ensure compliance with appropriate regulatory and quality requirements, and assisting with import-export activities
  • Represent clinical supply on cross-functional study teams, supporting product and company goals, while managing budget responsibilities and processes related to global clinical supplies
  • Manage acquisition, labeling, packaging, shipping, and management of any comparator drugs or other drugs co-administered with Elevar compound(s)
  • This role may require working outside normal business hours to ensure service to our global clinical network
Requirements
  • Bachelor’s degree in an engineering or scientific field with 12 years’ experience in clinical supply, including support of late-stage clinical development programs
  • Knowledge of cGxP (GMP, GLP, GCP etc.), IRT, and relevant quality systems
  • Packaging and label CMO management experience
  • Effective communication skills including written, verbal, and presentation skills
  • Ability to demonstrate Elevar’s core values by holding ourselves and each other accountable for the work we do, taking time to collaborate effectively while working remotely, making space for ingenuity in work and thought, and staying grounded in compassion

The anticipated annual base salary range for this role is $150,000 to $185,000. Final compensation depends on multiple factors including but not limited to, relevant experience, skillset, depth and breadth of knowledge, internal equity, and external market factors. Elevar Therapeutics is a rapidly growing biotech company that offers competitive wages and benefits package including medical, dental, vision, time off, a retirement plan, and other voluntary benefits for employees.

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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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