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About Cobalt:Cobalt is the data research lab shaping the frontier of artificial intelligence. We connect AI research teams with the expert data they need to build intelligent systems at scale across healthcare, life sciences, and robotics.About the role:Cobalt is seeking experienced clinical research professionals with direct experience contributing to Clinical Study Reports (CSRs). This project-based role is suited to clinical scientists, clinical development professionals, medical writers, research scientists, and other specialists who understand how clinical trial evidence is interpreted and communicated. The work may involve reviewing clinical research materials, evaluating the accuracy of clinical content, and drafting or revising sections of study documentation. Candidates do not need to be career medical writers, but they must have made a meaningful contribution to at least one CSR.ResponsibilitiesDepending on the project, you may:Review clinical trial protocols, statistical analysis plans, tables, listings, figures, and supporting documentsDraft, review, or revise sections of Clinical Study ReportsSummarize study design, methodology, patient disposition, efficacy, and safety findingsAssess whether written conclusions are supported by the underlying clinical evidenceIdentify inconsistencies between source documents, data outputs, and narrative contentEvaluate clinical research content for accuracy, clarity, completeness, and scientific validityIncorporate feedback from clinical, statistical, medical, and regulatory stakeholdersQualificationsDirect experience authoring, contributing to, or substantively reviewing at least one Clinical Study ReportStrong understanding of clinical research and clinical trial reportingAbility to interpret study documentation and clinical data outputsExcellent scientific writing, editing, and analytical skillsStrong attention to detail and commitment to factual accuracyAbility to work independently and meet project deadlinesAdvanced degree in a relevant scientific, medical, pharmaceutical, public health, or life sciences discipline preferredExperience tech, medical devices, a CRO, or clinical development preferredEngagement details:Project-based independent contractorFullyScope, timing, and compensation agreed upon for each projectPotential for additional projects based on performance and availability
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