Associate Director, Supply Chain, Logistics

🔥 13 hours ago

🏄 California – Remote

🏄 California – Remote

💵 $180.5k - $199.5k / year

⏰ Full Time

🟠 Senior

🔗 Supply Chain

👻 Ghost score 0%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Atrium Therapeutics

WebsiteLinkedInAll Job Openings

11 - 50 employees

Founded 2026

🧬 Biotechnology

💊 Pharmaceuticals

Biotechnology • Pharmaceuticals

Atrium Therapeutics is a clinical-stage biotechnology company developing precision RNA medicines targeted to the heart. The company has a proprietary RNA delivery platform built on clinically validated AOC (antibody-oligonucleotide conjugate) technology originally designed at Avidity Biosciences, enabling delivery of oligonucleotide therapies directly into cardiac muscle while addressing cytotoxicity, immunogenicity, and redosing limitations. Atrium's pipeline includes lead candidates ATR-1072 for PRKAG2 syndrome and ATR-1086 for PLN cardiomyopathy, plus additional research-stage targets in rare cardiomyopathies; the company plans to file an IND for ATR-1072 in the second half of 2026. Atrium positions itself to pioneer precision cardiology by bringing RNA therapeutics to patients with genetic and rare forms of heart disease.

📋 Description

• Provide strategic direction for clinical supply strategies and create actionable clinical supply plans • Manage IRT/RTSM vendors, specification gathering, user acceptance testing, and IRT lifecycle • Ensure accurate randomization, resupply, and inventory levels across studies and sites • Identify and mitigate clinical supply risks and build contingency plans • Align clinical supply timelines with study start-up, enrollment, and closeout milestones • Oversee packaging, labeling, distribution, and return drug management with CMOs • Represent Clinical Supply Chain in cross-functional study team, CRO, and vendor meetings • Author pharmacy manuals and participate in study-document reviews • Own shipping and logistics requests for GMP and non-GMP materials across technical and scientific teams • Manage couriers, freight forwarders, and specialty cold-chain carriers • Own import/export compliance, licenses, permits, customs documentation, and country-specific import requirements • Oversee cold-chain shipment execution, packaging qualification, temperature excursion investigations, and corrective actions • Monitor shipment status, coordinate inbound/outbound logistics, resolve delays or exceptions, and maintain tracking/reporting • Ensure compliance with GMP, GCP, and applicable import/export regulations • Maintain inspection-ready documentation and file records in eTMF/quality systems • Support SOP creation and revision • Lead or contribute to deviation, CAPA, and investigation processes related to supply or shipping issues

🎯 Requirements

• Bachelor's degree in life sciences, supply chain, logistics, or a related field required; advanced degree preferred • Associate Director: typically 10+ years of clinical supply chain experience in biotech/pharma • Direct experience in packaging, labeling, and distribution of investigational products through all stages of international clinical studies • Experience managing shipping, logistics, or distribution operations, including carrier/freight-forwarder management and import/export or customs compliance • Experience with IRT/RTSM systems, clinical supply forecasting tools, and CMO/depot network management • Experience in rare disease, cardiology, or genetic medicine clinical trials is a plus • Working knowledge of GMP, GCP, and global import/export regulations relevant to clinical trial materials • Strong vendor management, negotiation, and cross-functional collaboration skills • Ability to manage multiple competing priorities in a fast-paced, growing biotech environment • Excellent analytical, organizational, and written/verbal communication skills • Comfort operating with the autonomy and hands-on scope typical of a small, growing company • Some domestic and/or international travel may be required to support vendor, depot, or CMO site visits • Role based in San Diego, CA or remote

🏖️ Benefits

• Stock options & RSUs • 401(k) with employer match • Medical coverage • Dental coverage • Vision coverage • LTD coverage • Unlimited time off, including summer & winter breaks • Learning and development programming • Job-specific industry training opportunities • Education reimbursement program