Pattern Bioscience

• Receive ad-hoc requests for information and promptly respond with accurate information • Translate business needs to technical specifications • Write efficient SQL queries to interrogate data • Create stunning graphs/reports/dashboards using Tableau • Proven abilities to take initiative and be innovative • Coordinate with Analytics team in US with weekly planning • Work with all levels of end users, including executive staff • Dive into data issues when questions arise and offer solutions • Conduct unit testing and troubleshooting.

Role Description To prepare for and manage clinical studies for our diagnostic assays, we are hiring a Senior Clinical Research Associate to join our Clinical Affairs team. In this role, you will support external studies, including site selection, site initiation visits, and routine monitoring. Serving as the liaison between clinical sites and Pattern teams, you’ll have the opportunity to collaborate across the organization including with Assay Development, Hardware, Software, Quality, and Regulatory. This role is for you if you enjoy combining your passion for infectious disease or diagnostics with organizational and communication skills to support building new partnerships with clinical study sites. How You Will Contribute - Set up and support sites for clinical trials and other external studies—including providing training, maintaining close communication, organizing study documents, and helping with study logistics. - Optimize clinical study workflows and implementation. - Ensure studies are conducted, monitored, and documented according to GCP and Pattern Bioscience SOPs. - Assist in the build and validation of electronic data capture systems. - Review/monitor data from active external studies, ensuring all errors are caught and queries appropriately resolved. - Collaborate with Pattern’s R&D and/or Microbiology teams. - Contribute to drafting SOPs, study manuals, and other clinical documents. We'd Love to Hear from You If You - Self-prioritize work effectively, applying strong organizational skills. - Demonstrate attention to detail and accuracy when delivering and following instructions and when reviewing and generating data and documents. - Are teachable and love new challenges and learning new technology. - Adapt quickly to changing priorities, timelines, and goals; are flexible with shifting strategies; and think nimbly to generate creative solutions. - Love developing and creating organizational infrastructure. - Have strong communication skills. - Have a customer-centric mindset. Goals - 90 days: - Become familiar with Pattern technology and assay/instrument workflows. - Perform site/data monitoring for clinical studies. - Organize and maintain study documents and data files. - Contribute to qualification of potential clinical study sites for upcoming studies. - Help coordinate clinical specimen shipments from clinical partners to Pattern. - Participate in Clinical Study preparedness activities. - Participate in study site start-up activities. - 6 months: - Support Pneumonia ID/AST clinical study initiation at external sites. - Organize Pneumonia ID/AST clinical study master files. - Support set up and execution of analytical validation studies (e.g., reproducibility study). - Build strong relationships/credibility with other internal teams as well as external clinical sites/vendors. Qualifications - B.S. in biological sciences, medical laboratory science, or related field. - 3-5 Years' experience in actively managing multi-site diagnostic device clinical trials, managing clinical study documentation/clinical study master files. - Knowledge of GCP and FDA regulations related to conducting IVD/device clinical trials. - Hands-on lab experience in microbiology and applied knowledge of bacteriology (a plus). - Experience working with clinical specimens and microorganisms (a plus). - Working knowledge of general workflows in a clinical microbiology laboratory, including Gram-stains, organism identification, conventional culture, and AST (a plus). - Knowledge and experience in performing and interpreting antibiotic susceptibility testing (AST) (could be in an industry, research, or clinical laboratory setting) (a plus). Requirements - Average of 50% travel required with up to 75% travel during peak times. - Type of Position: Exempt, Full-time. Benefits - Health insurance. - 401k Matching. - Paid Time Off. - The opportunity to make a global impact.

• Manage, build, and grow partners’ eCommerce activities on Coupang, Naver, and other marketplaces • Drive revenue growth on marketplaces in Korea through a data-driven approach across a portfolio of brands • Develop and implement the strategy and joint business plan with brands • Oversee the eCommerce channels’ operation and campaign delivery by leading cross-functional teams • Establish and maintain relationships with client partners • Conduct analysis of brands performance using multiple data sources to ensure performance optimization • Lead and setup the Korea eCommerce operation and marketing team • Partner with logistic team to manage cross border and domestic fulfilment