This individual will guide efforts to increase productivity through innovative solutions, support and/or manage the BSO systems and tools within the Biorepository and Clinical Study Management teams and is responsible for the integrity of Denali's valuable clinical biospecimen collection, and associated data, to enable Denali's goals. This is achieved through oversight of BSO staff, hands-on work, collaboration with other functions and continuous improvement of BSO procedures and practices. Key Accountabilities / Core Job Responsibilities • Management of software containing clinical biospecimen data in close collaboration with Biorepository staff, Clinical Study Management, Data Management and Clinical Programming • Responsible for ongoing maintenance and improvements of BSO systems and tools, as necessary • Ensure sample integrity and maintain GCP and GDPR compliance for clinical trial samples through chain of custody, sample handling guidelines, and proper storage conditions • Responsible for design and build of study collection plans to allow real-time import of incoming samples into LIMS. This requires coordination with scientists, CROs and vendors and ability to interpret clinical research protocols. • Responsible for vendor management and oversight of BSO managed vendors • Mentor and train BSO staff, train relevant functional groups in BSO procedures, and participate in the creation and updating of BSO SOPs • Management of biomarker studies and collaborations, and support of clinical study management projects • Lead process improvement projects to enable efficiency and innovation in BSO processes • Review and approve Data Transfer Specifications, custom manifests, import files, and other sample data collection documents Qualifications/Skills • Bachelor's degree in Biochemistry, Chemistry, Biology, Immunology, Medical Technology or related field, with a minimum of 5 years of experience in Translational Medicine or Clinical Development, or related field/training • Experience with human biosample management, regulatory compliance, and quality assurance in a clinical trials/drug-development setting • Proficient in LIMS database entry, advanced Excel, and interpreting Clinical Research Protocols • Ability to work effectively in a cross-functional team matrix environment • Strong customer-service focus with advanced planning and organizational skills; adapts quickly to shifting priorities and deadlines Salary Range: $114,000.00 to $149,000.00 . Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more at https://www.denalitherapeutics.com/careers This compensation and benefits information is based on Denali’s good faith estimate as of the date of publication and may be modified in the future.