Remote Diabetic Retinal Screening Jobs in California

Clinical Supply Specialist (Contract)Remote, United States4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company's lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company's lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company's second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol deliveryGeneral SummaryReporting to the Director, Supply Chain, this role is expected to work closely within the Supply Chain team, as well as cross-functional groups such as Clinical Operations and Quality. This is a remote or hybrid position.ResponsibilitiesSupports the development and execution of Clinical Supply strategies for all 4DMT's Phase 1/2/3 investigational drug products and ancillariesCoordinate and track bulk drug orders to ensure adherence to pre-defined supply and resupply timelinesMonitor site inventory on a daily basis; coordinate and track drug shipments to ensure uninterrupted supplySupports drug product inventory management and distribution in partnership with 4DMT's clinical partners; evaluates drug utilization versus forecast considering country requirements and logistical timelineMaintains study and depot-level accountability and reconciliation documentation to support regulatory compliance and study closeoutTracks and resolves study and depot level temperature excursions. Provide routine reporting of drug wastage due to these excursionsArchives Proof of Delivery (POD) documentationMaintain traceable documentation to support GXP activitiesArchives documentation on Trial Master Files as requiredQualificationsEducation and Experience:Degree in biological or life sciences, pharmacy or medicine (or international equivalent). A minimum of 3 years in the pharmaceutical industry or relevant work experience and a minimum of 1 year in Clinical Supply Chain.Familiar in the daily management and operations of a Clinical Supply Chain inclusive of bulk management, distribution, and maintaining study blinds across multiple investigational productsExperienced with Interactive Response Technology - IRT systems for inventory management and resupplyWorking knowledge of regulations relating to clinical labeling, packaging, and distribution activities; working knowledge of GMP/GCP/GLP regulationsSkills:Intermediate/Advanced knowledge of Microsoft SuitesKnowledge of Clinical Supply ManagementSolid written and verbal communication skillsExcellent planning and organizational skills and the ability to work simultaneously on multiple projects with tight timelinesExcellent interpersonal and communication skillsPositive attitude with a strong desire for continuous learningHourly compensation range: $58.00 - 70.004DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws. Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities