Source Job

$190,989–$231,434/yr
United States 4w PTO

  • Own clinical supply chain order fulfillment, including labeling, packaging, and distribution of trial products.
  • Build and lead Clinical Supply Chain, Planning, and Warehousing teams with full regulatory compliance.
  • Develop sourcing strategies and manage vendors to ensure cost-effective, uninterrupted supply.

Supply Chain Management Procurement Demand Planning Regulatory Compliance Vendor Management

8 jobs similar to Director, Clinical Supply Chain & Planning

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US

  • Manage end-to-end supply chain for specialty medications and clinical supplies across infusion clinics.
  • Develop and maintain inventory processes, including ordering controls, par-level optimization, and waste reduction.
  • Partner with finance, pharmacy, and manufacturer relations to evaluate purchasing opportunities and contract performance.

Nira Medical is a national partnership of physician-led, patient-centered independent practices dedicated to advancing neurological care. They support practices with cutting-edge technology, clinical research, and a collaborative network, scaling their teams and services as they grow.

US Unlimited PTO

  • Manage clinical study vendors and ensure deliverables are on time, within budget, and compliant with FDA and ICH/GCP guidelines.
  • Support CRO collaboration, site start-up, study documentation, and risk mitigation with cross-functional teams.
  • Leverage AI tools and process improvements to enhance clinical operations productivity and quality.

This biotechnology company focuses on developing innovative oncology therapies. It offers a collaborative, multidisciplinary environment with opportunities to use AI-enabled tools and modern approaches to clinical operations.

$155,000–$195,000/yr
North America

  • Support planning and operational execution of clinical trials, coordinating across sites, CROs, vendors, and teams.
  • Manage vendor oversight, budgets, timelines, risks, and documentation ensuring GCP compliance.
  • Serve as primary operational contact and mentor junior staff for global Phase 1-3 trials.

Jade Biosciences is a clinical-stage biotechnology company developing best-in-class therapies for autoimmune diseases. It is a small, dynamic company offering an exciting opportunity to contribute to its immunology pipeline.

US Unlimited PTO

  • Collaborate with the Clinical Operations team to support timely conduct of clinical studies according to protocols, GCP, SOPs, and regulations.
  • Lead operational management for assigned regions and sites, including vendor management and oversight of CRO monitors.
  • Contribute to the development and maintenance of study documents and ensure the Trial Master File is complete and inspection-ready.

BridgeBio is a biopharmaceutical company founded to discover, create, test, and deliver transformative medicines for patients with genetic diseases and cancers with clear genetic drivers. Founded in 2015, the company has built a portfolio of 20+ drug development programs spanning preclinical to late-stage development across multiple therapeutic areas.

$85,000–$115,000/yr
US

  • Support Clinical Trial Managers with study start-up, protocol development, and Trial Master File preparation.
  • Coordinate with clinical sites on documentation, training, and compliance with FDA and GCP requirements.
  • Assist with tracking study payments and providing operational support across the full study lifecycle.

The company is a partner organization specializing in clinical research and development, operating through Jobgether. It offers a structured clinical operations environment with cross-functional teams and professional growth opportunities.

$173,000–$320,000/yr
US

  • Provide medical direction and oversight for clinical trials, including safety monitoring and medical data review.
  • Partner with GCO to build client relationships and support proposals, feasibility, and business development.
  • Serve as drug development SME, contributing to protocols, training, and medical strategy across studies.

Fortrea is a global contract research organization providing clinical development and trial management services to pharma/biotech. It fosters a collaborative, family-like culture focused on advancing life-saving therapies.

$90,000–$140,000/yr
US

  • Monitor clinical trial sites to ensure compliance with protocols, SOPs, and regulatory requirements.
  • Review electronic medical records and source documentation for accuracy and data integrity.
  • Support site staff and contribute to development of trial materials, SOPs, and training guides.

Orca Bio is a commercial-stage biotechnology company developing next-generation cell therapies to improve transplant outcomes for blood cancer patients. The company maintains a start-up culture with an entrepreneurial spirit and emphasis on camaraderie.

Global

  • Lead and oversee global clinical trials from inception to closure, managing cross-functional teams and vendors.
  • Ensure compliance with ICH/GCP and regulatory standards while driving recruitment and risk management strategies.
  • Manage study materials, systems (EDC, IRT, CTMS), and provide training to stakeholders.

AbbVie is a biopharmaceutical company focused on discovering and delivering innovative medicines in immunology, oncology, neuroscience, and aesthetics. With a global presence, they emphasize integrity, innovation, and community service.