ADARx Pharmaceuticals Inc. · 18 hours ago
Supply Chain Specialist
San Diego, CA, San Diego, CA, US
Full-time
Onsite
Mid Level
$87K/yr - $115K/yr
3+ years expADARx Pharmaceuticals, Inc. is a clinical stage biotechnology company dedicated to transforming cutting-edge science into next-generation RNA therapeutics. They are seeking a Supply Chain Specialist to support planning, coordination, and execution of global clinical supply activities for clinical trials, ensuring compliance with regulatory requirements and maintaining supply chain efficiency.
BiotechnologyHealth CareMedicalPharmaceutical
Responsibilities
Develop and promote a workplace culture that values diversity of thought, promote integrity and create an atmosphere that supports coaching and fosters accountability
Carry out assigned laboratory functions applying knowledge and skill in an accurate, timely manner
Establish and maintain excellent working relationships with critical collaborative partners throughout the company
Support end-to-end clinical supply chain activities including forecasting, planning, packaging, labeling, distribution, returns, and reconciliation of investigational product
Coordinate with internal stakeholders and external CMOs, depots, and logistics vendors to ensure timely manufacturing and delivery of clinical supplies
Maintain and track inventory levels at depots and sites; proactively identify and mitigate potential supply risks
Generate and manage clinical supply forecasts and resupply strategies based on enrollment projections, drug product expiry dates, and study timelines
Support creation and review of packaging and labeling specifications in alignment with study protocols and regulatory requirements
Manage Interactive Response Technology (IRT/RTSM) supply settings and ongoing updates in collaboration with Clinical Operations and vendors
Prepare and review shipment documentation and ensure compliance with import/export and country-specific requirements
Reconcile clinical supplies, including returns, destructions, and accountability documentation
Contribute to development and continuous improvement of SOPs, work instructions, and supply chain processes
Ensure all activities comply with GCP, GMP, and applicable regulatory guidelines
Maintain accurate documentation and support audits and inspections as needed
Provide Operational support services to CMC development and manufacturing functions
Reviews and recommend updates for departmental SOPs, may draft updates to SOPs depending on experience and level
Maintain all appropriate corporate standards for facility safety and hazardous material management
Other duties as assigned
Qualification
Required
Bachelor's degree in supply chain, life sciences, or related field
BS with 3 years of experience or MS with ½ years of experience in clinical supply chain, clinical operations, or pharmaceutical logistics
Excellent organizational, written and verbal communication skills; and effective presentation of complex scientific data to cross-functional and senior management teams are essential for this role
Working knowledge of GxP requirements and global clinical trial supply practices
Experience coordinating with CMOs, depots, and third-party logistics providers
Familiarity with IRT/RTSM systems and clinical supply management tools
Strong organizational skills with the ability to manage multiple studies and priorities simultaneously
Proficient in Microsoft Office (Excel, Word, PowerPoint); experience with ERP or inventory systems preferred
Must be able to work independently with supervision as needed
Proficient at working independently as well as in cross-functional team settings
Adaptable / Flexible - willing and able to adjust to multiple demands and shifting priorities as well as an ability to meet day-to-day challenges with confidence and professionalism
Self-motivated with excellent interpersonal, organizational and communication skills with the ability to take a hands-on approach to work effectively in a dynamic and collaborative, fast-paced environment
Strong problem-solving skills and a proactive attitude towards exploring new approaches
Understanding of project timelines and deliverables and plans/coordinate project work accordingly with departmental, functional, and external stakeholders
Preferred
Experience supporting global, multi-site clinical trials (Phase I–III)
Understanding of temperature-controlled shipping and cold chain management
Experience with import/export documentation and international shipping regulations
Prior experience in a small to mid-size biotech or fast-growing pharmaceutical company
Benefits
Equity-based compensation
Performance-based bonuses
401(k) with Company Match
Medical, Dental, Vision
Flexible Spending Account
Life Insurance
Employee Assistance Program
Employee Discounts
Gym Membership
Paid Vacation
Paid Holidays
Paid Sick, Jury Duty, Bereavement
Company
ADARx Pharmaceuticals Inc.
ADARx Pharmaceuticals, Inc., located in San Diego, is a clinical stage biotechnology company committed to turning cutting-edge science into life-saving therapeutics.
51-200 employees
Funding
Current Stage
Growth StageTotal Funding
$332MKey Investors
LG Technology VenturesBain Capital Life Sciences,TCG CrossoverAscenta Capital
2025-02-01Series Unknown
2023-08-09Series C· $200M
2023-01-20Series B· $46M
Leadership Team
Ajim Tamboli
Chief Financial Officer
Donald Fong
Chief Medical Officer
Recent News
2026-02-07
2026-01-16
Company data provided by crunchbase