Senior Clinical Trial Manager

Senior Clinical Trial ManagerRemote; Seattle, Washington, United StatesUmoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals. We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.Umoja Biopharma – Your Body. Your Hope. Your Cure.Position SummaryThe Senior Clinical Trial Manager is primarily responsible for the operational management and oversight of Umoja's clinical studies. This individual will work closely with Clinical Operations leadership, Medical Director(s), other cross-functional team members, and designated CROs to ensure the successful completion of all clinical study activities and project deliverables within specified quality, time, and cost parameters.The ideal candidate brings clinical operations expertise in biotech and the ability to thrive in a fast-paced, entrepreneurial environment.This role is ideally based out of our Seattle, WA location and is onsite at least 2 days/week. We are open to remote work within the US for the right candidate.Core AccountabilitiesSpecific Responsibilities Include:Ensures studies are carried out according to the study protocol, SOPs, and ICH/GCP guidelines/regulations and study specific manuals and proceduresIndependently develop study timelines, key deliverables, and risk/mitigation strategiesLead selection and performance management of CROs and other ancillary vendors during study start-up, conduct, and close-outPlan and lead study team meetingsLead the development of study materials (e.g., study plans, monitoring guidelines, site initiation visit materials, site tools and worksheets)Contribute to the content and review of study documents (e.g., protocol, informed consent forms, case report forms (CRF), CRF completion guidelines, product administration guidelines)Track and ensure optimization of site startup activities and activation, subject enrollment, data collection, and trial closeoutEnsure accurate and timely execution of site visit monitoring reportsIdentify, select, and monitor performance of sitesNegotiate and manage the budgets and payments for sitesDevelop and maintain strong working relationships with study investigators and site staffManage investigational product release packages and investigational product accountabilityCoordinate with Clinical Supply Chain Operations regarding investigational product shipment to sitesOversee the Trial Master File according to ICH-GCP and SOPsMay assist in clinical data review and query generationCollaborates closely with Clinical Operations, Clinical Development, Biometrics, Clinical Data Management, Regulatory Affairs, Translational Medicine, Clinical Supply Chain, Pharmacovigilance, and Clinical Quality AssuranceActively participate in and contribute to the development of department initiatives aimed at improving efficiency and best practicesThe Successful Candidate Will Have:Manager Level: Bachelor's degree or equivalent in Life Sciences with at least 6 years of clinical operations experience in the pharmaceutical industry with at least 1 year experience managing industry-sponsored pharmaceutical clinical studies as a sponsor employeeSenior Manager Level: Bachelor's degree or equivalent in Life Sciences with at least 8 years of clinical operations experience in the pharmaceutical industry with 3+ years' experience managing industry sponsored pharmaceutical clinical trials as a sponsor employeeSignificant knowledge of GCP/ICH guidelines and the clinical development processAbility to plan, organize and conduct clinical studies with minimum oversightSignificant experience managing CROs and other vendors and assessing performanceExperience leading, managing, or mentoring clinical operational staff and cross-functional teamsStrong organizational skills and the ability to balance changing prioritiesStrong interpersonal and communication (written and verbal) skillsDemonstrated ability to work independently and as part of a multi-functional teamAble to solve problems under pressureSelf-motivated and able to work effectively in a matrix/team environmentPreferred Qualifications:Experience supporting Phase 1 and 2 clinical trials is preferredOncology experience is highly preferredPhysical Requirements:Ability to travel as needed (approximately 20%)Ability to work onsite 2 days/week at our Seattle, WA officeAbility to sit for prolonged periods of timeManager Level Salary Range: $125,000 - $150,000 Senior Manager Level Salary Range: $150,000 - $175,000Benefits OfferingsUmoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the Benefits section of our website.