OverviewLos candidatos deben tomarse el tiempo de leer atentamente todos los elementos de este anuncio de empleo. Por favor, envíen su solicitud sin demora.As a Clinical Scientist Director in Early Development Oncology, you translate scientific strategy into actionable clinical execution in early-phase trials. You provide hands-on oversight of protocol execution, data quality, and medical data review to enable decision-ready data. You collaborate across cross-functional teams to align trials with protocol intent, regulatory expectations, and Amgen standards. You contribute medical monitoring, data interpretation, and governance with CROs and external partners. This role offers the chance to shape oncology development and impact patient outcomes within a collaborative, science-driven culture.Compensaciones / BeneficiosRetirement and savings plangroup medical, dental and vision coveragelife and disability insurancediscretionary annual bonus programstock-based long-term incentivesflexible work models (remote and hybrid)ResponsabilidadesOversee protocol execution and data quality in early-phase oncology trialsContribute to medical monitoring and assessment of subject-level data to identify risks and issuesCollaborate across cross-functional teams to translate clinical strategy into study concepts and documentsProvide guidance in managing collaborators, consultants,



and CROs for key projectsEnsure protocol integrity and governance for clinical plans and final deliverablesReview and analyze trial data for accuracy, regulatory compliance, and completenessConduct data quality assessments within a data monitoring plan across the trial lifecycleSupport regulatory submissions and high-level clinical regulatory responsesDraft and contribute as an author to publications and conference presentationsUtilize data analysis tools (e.G., Spotfire) for clinical data interpretationRequisitos principalesDoctorate, 4+ years in life sciences/healthcare OR Master’s, 7 years OR Bachelor’s, 9 years (substantial clinical drug development experience)Experience in pharmaceutical early-phase oncology development xhfqzwm Strong communication and presentation skills for leadership audiencesExperience designing, monitoring, and implementing oncology clinical trials under GCPAbility to perform data readouts, data cleaning, and outputs for regulatory or internal useExperience drafting regulatory submission materials and responsesContributing author experience for scientific publications and conferencesFamiliarity with Spotfire or similar data analysis toolsclear communicatorcross-functional collaborationproblem solvingclinical trial design and executiondata interpretation and statistics basicsGCP regulatory knowledge

📌 Clinical Scientist Director, Early Development Oncology - Amgen (Muxía)
🏢 Jobrapido
📍 Muxía