Spencer brings significant expertise with over 23 years in drug development and commercialization experience across large and small biotech. He has dedicated more than 12 years of his career to amyloid-related diseases, including AL and ATTR amyloidosis, Alzheimer’s and Parkinson's disease, and has authored over 30 scientific publications in amyloidosis.
Prior to Attralus, he was VP, Head of Global Strategy for ATTR Amyloidosis at Akcea and Ionis. Prior to that, he was VP, Head of Development Operations and Medical Affairs for Prothena Biosciences leading programs in AL and ATTR Amyloidosis. In addition, Spencer has significant leadership experience in clinical development, portfolio program management and as a Project Team Leader at Genentech, Elan, Janssen and Ultragenyx working to bring >15 new therapeutic candidates through IND, >10 to phase 3, and 6 products to the market.
Spencer has a BS in Neuroscience from Vanderbilt University, an MPH in Outcomes Research from Johns Hopkins School of Public Health, and an MBA from the Paul Merage School of Business at University of California.
Jonathan Wall is a Professor at University of Tennessee Medical Center, Knoxville and Head of the Amyloidosis and Cancer Theranostics Program. Jonathan is an internationally known expert in the field of amyloidosis, has worked in amyloid based research for over 20 years.
He has over 100 publications and more than 13 issued US patents in this field. His research work was instrumental in the development of multiple antibody-based therapeutics that have undergone clinical development by biotech companies. His lab has received over $10M in NIH grant and contract funding for work that focuses on the development and translation of novel diagnostic and therapeutic reagents for amyloidosis.
Benson has over 30 years of experience in financial and business development activities in life science companies. He is a consulting CFO to startups and has served as Interim CFO at E-Scape Bio, ReCode Therapeutics, and GABAeron. Prior to this, he served as CEO of Lapis Pharmaceutical as well as Senior VP Corporate Development at CoTherix where he was responsible for in-licensing Ventavis® (iloprost) which was later FDA approved and successfully launched.
Benson’s prior experience also includes being the first VP for venture debt lending at Imperial Bank/Comerica, serving as CFO at Cibus Pharmaceutical, Controller at Matrix Pharmaceuticals, and Division Controller in Express Banking at Wells Fargo Bank. He was also a tax accountant and CPA at Arthur Young & Co. after he received his BS in Biology from the University of Oregon. His responsibilities have included filing S-1s, equity and debt financing and product licensing.
Scott has more than 35 years of experience working in biotech and pharma, with deep expertise in CMC development and the manufacturing of a wide range of therapeutic product types including small molecules, hormones, and other therapeutic proteins, such as monoclonal and bispecific antibodies, oncolytic viruses, cytotoxic prodrugs, cancer vaccines, and therapeutic plasmids. Through his years of experience, Scott has served in senior executive roles managing CMC development and manufacturing operations as well as Regulatory Affairs, Quality, Project Management, and Product Development functions. He has facilitated the development of several products through preclinical and clinical development to commercialization.
Prior to joining Attralus, Scott served as Vice President of Technical Operations at Protein Design Labs; Senior Vice President, Head of Product Development at Onyx Pharmaceuticals; Vice President of Manufacturing and Process Development at BioMarin; Vice President of Technical Operations at Xencor; and Head of CMC at Bavarian Nordic. Scott earned an M.S. in Microbiology at Texas A&M University and a B.S. degree in Microbiology from University of Louisiana at Lafayette.
Attralus, Inc., (formerly Aurora Bio) is a VC funded privately held development stage biotechnology company focused on improving the lives of systemic amyloidosis patients, through the development of novel diagnostics and therapeutics. We are developing pan-amyloid targeting agents that facilitate diagnosis, and the development of novel immunotherapies designed to clear amyloid fibrils in patients with systemic amyloid diseases. We aim to improve the diagnosis and treatment of systemic amyloid diseases, such as light chain (AL), transthyretin (ATTR), and LECT2 amyloidosis, to increase patient survival and quality of life.
Attralus’ technology has broad applications and the potential to address up to 30 systemic amyloid based diseases. Attralus has a diagnostic imaging agent currently in a ph 1/2 trial, positioned to potentially be the first approved diagnostic specifically for amyloidosis. The company also has 2 novel therapeutic fusion proteins, directed at amyloid removal, that are in pre-clinical development
Headquartered in South San Francisco and founded in 2019, Attralus has recently completed a Series A funding with VenBio to carry forward its mission to improve the lives of systemic amyloidosis patients
The AD/Director, Program Management will be responsible for providing both strategic and hands-on program and project management expertise. Initially reporting directly to the CEO, the AD/Director will be responsible for creating the program plan and budget and providing daily coordination and tracking of critical activities, assuring all milestones and deliverables are met. The Director will be responsible for developing the program management processes and procedures for the company, determining appropriate software and other tools, structuring regular meetings and communication within the company and with external collaborators.
• Collaborate with the management team to provide project management leadership and execution activities within the company and between external partners and Attralus teams.
• Develop and execute integrated cross-functional project plans with established goals, milestones, timelines and budget, with a key focus on bringing pre-clinical therapeutic programs into early clinical development
• Conduct and direct day-to-day program activities to meet milestones; monitoring critical path activities to ensure delivery of program objectives.
• Drive planning for key drug development milestones.
• Maintain effective communication with the management team through oral and written correspondence and ensure adequate documentation of each communication.
• Always use/model/maintain/promote best practices in Program Management, including the use of agendas, minutes, dashboards, maintain document repository, establish and implement templates, tools, and processes to drive efficiency, alignment, communication, and effective planning.
• Create and maintain easily accessible, high level program documents in electronic format.
• Recommend, manage and train on necessary software and tools.
• Identify, develop and/or maintain an appropriate electronic platform (SharePoint, Shared Folders, etc.) for reporting/archiving/documentation of relevant program information, records, etc.
• Conduct risk management, contingency and scenario planning using appropriate program management tools.
• Identify program issues or resource gaps and facilitate resolution.
• Communicate program information and support development of program presentations to senior leadership, board members, investors and other key stakeholders as appropriate.
• Contribute to budgetary planning at the program level.
• Facilitate adherence to Aurora’s governance processes; work with key stakeholders to prepare for those interactions; lead/support as appropriate. Ensure implementation of governance decisions.
• Minimum of a BA/BS in a scientific disciplined is required, Advance degree preferred
• 7+ years of program management or equivalent experience in a pharmaceutical or biotechnology organization.
• Experience with research/pre-clinical and early clinical development project planning required. PM Certification is a plus.
• Rare disease experience a strong plus (not required).
• Desire and ability to work in a start-up, fast paced organization where you will wear many hats.
• Must have excellent verbal and written communication skills as well as exceptional organizational capability.
• Ability to drive program plans and timelines (across multiple functional areas) is essential. Proven success in goal setting, prioritization and time management is required.
• Understanding of FDA and/or EMA quality and regulatory processes. Prior experience with regulatory filings is desirable.
• Experience working with external partners is desirable.
• Ability to work independently in decision-making and resolution of program obstacles and conflicts.
• Familiarity with developing budgets and forecasting is desirable.
• Ability to function autonomously, with an appreciation of detail while being cognizant of “the big picture.”
• Have a patient-first mindset. All decisions made with patients in mind.
• Proficiency with Microsoft Word, Excel, PowerPoint, and Project is required.
Benefits/Equal Opportunity Employer
Attralus, Inc. offers both comprehensive benefits and Paid Time Off (PTO) plans for employees, which begin on the first day of employment.
Attralus, Inc. is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.