Lead clinical project delivery at Altasciences through timeline management, stakeholder communication, and risk planning. This position requires approximately 10% travel.The Scientific Project Manager independently executes clinical projects from study award through archival. You will coordinate internal and external teams, manage client relationships, and oversee third party vendors. The work includes budgets, regulatory compliance, study documentation, and critical path management.Key Responsibilities:
Develop timelines and proactively manage critical project pathsCoordinate meetings, action items, stakeholders, and client communicationsManage vendors, contracting, milestones, billing, and change ordersCoordinate clinical documents, submissions, sites,
and Trial Master FilesConduct budget reconciliations and provide project accrualsRequirements:
Bachelor degree or higher in sciences or related fieldsMinimum four years of clinical, nonclinical, or CDMO experienceMinimum two years of related project management experienceWorking knowledge of Microsoft Office and project systemsAbility to communicate fluently in EnglishApply scientific project management expertise to clinical timelines, vendors, regulatory documents, budgets, and stakeholder delivery at Altasciences.
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