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O SkillsMP coletou 99 skills de nroze22/TalosixSkills. Abra uma skill para revisar a origem e os detalhes.
nroze22/TalosixSkillsMostrando 40 de 99 skills coletadas.
Production incident response framework for Talosix EDC systems. Covers severity classification with patient safety considerations, investigation steps, root cause analysis, communication templates, and CAPA follow-up.
Idioma do texto original: inglês
Design and execute load testing plans for Talosix EDC systems with performance benchmarks, tool setup (k6, Artillery), result analysis, and concurrent clinical site user simulation.
Idioma do texto original: inglês
Generate marketing content tailored for clinical trial EDC audiences including blog posts, thought leadership articles, and social media content with industry-appropriate tone and SEO optimization.
Idioma do texto original: inglês
Analyze and optimize application performance for Talosix EDC systems. Covers database query optimization, caching strategies, frontend and backend profiling, and load testing recommendations.
Idioma do texto original: inglês
Generate Playwright automated test scripts for the Talosix EDC platform. Uses Page Object Model, data-testid selectors, and covers clinical trial UI patterns including forms, validation, and e-signatures.
Idioma do texto original: inglês
Converts Product Requirements Documents from Confluence into interactive HTML/React wireframe prototypes with clinical trial EDC patterns. Pulls PRDs via Atlassian MCP, extracts user stories and acceptance criteria, then generates a fully navigable prototype…
Idioma do texto original: inglês
Draft press releases for Talosix company news including feature launches, partnerships, funding, and awards following AP style and clinical trial industry conventions.
Idioma do texto original: inglês
Generate comprehensive PRDs for Talosix clinical trial EDC features, including regulatory considerations, user stories, and technical requirements.
Idioma do texto original: inglês
Guide safe refactoring in validated clinical trial systems. Performs impact analysis, regression risk assessment, and generates change control documentation for Talosix EDC software.
Idioma do texto original: inglês
Match Talosix reference customers to prospect profiles based on therapeutic area, study phase, company size, and geography, with talking points and usage tracking.
Idioma do texto original: inglês
Post-release monitoring plan for Talosix EDC deployments. Covers key metrics, alert thresholds, smoke test execution, and escalation procedures.
Idioma do texto original: inglês
Generate release notes from Jira tickets and git history in multiple formats (internal, customer-facing, regulatory) with compliance and validation impact statements.
Idioma do texto original: inglês
Create product roadmaps for Talosix EDC platform tailored to different audiences (engineering, leadership, customers) with timelines, dependencies, and milestones.
Idioma do texto original: inglês
Build custom ROI calculators for Talosix EDC prospects, factoring in study setup time, data query reduction, monitoring efficiency, and industry benchmarks to quantify the business case.
Idioma do texto original: inglês
Forecast Talosix pipeline and revenue with weighted pipeline analysis, historical conversion rates, and segmentation by deal type, customer type, and study phase.
Idioma do texto original: inglês
Build professional proposals for Talosix EDC and clinical trial software deals including executive summary, solution overview, pricing, implementation timeline, support model, and ROI projections.
Idioma do texto original: inglês
Generate comprehensive RFP responses for Talosix clinical trial EDC, addressing security questionnaires, vendor assessments, compliance certifications, and therapeutic area tailoring.
Idioma do texto original: inglês
Comprehensive security audit for Talosix clinical trial EDC software. Covers OWASP Top 10, HIPAA, 21 CFR Part 11, authentication, authorization, encryption, dependency scanning, and PHI protection.
Idioma do texto original: inglês
Create keyword-optimized content for clinical trial search terms including metadata, heading structure, internal linking strategy, and content briefs targeting EDC, clinical data management, eCRF, and CDMS keywords.
Idioma do texto original: inglês
Help plan sprints for Talosix EDC development with story point estimation, capacity assessment, sprint goal definition, and Jira integration.
Idioma do texto original: inglês
Create stakeholder alignment documents including RACI matrices, decision logs, and communication plans for cross-functional clinical trial feature development.
Idioma do texto original: inglês
Generate comprehensive test cases from Jira stories for Talosix clinical trial EDC platform. Produces positive, negative, boundary, and edge cases with regulatory coverage. Output is formatted for direct import into Zephyr Scale.
Idioma do texto original: inglês
Plan test cycles with resource allocation, entry/exit criteria, environment requirements, defect management, and regression test selection for the Talosix EDC platform.
Idioma do texto original: inglês
Create comprehensive test strategies for Talosix EDC platform releases. Covers risk-based testing, all test levels, regulatory validation (IQ/OQ/PQ), and resource planning for clinical trial software.
Idioma do texto original: inglês
Generate UAT test suites for CRO and sponsor users of the Talosix EDC platform. Produces business-language test scripts covering clinical workflows with clear pass/fail criteria. Formatted for Zephyr Scale.
Idioma do texto original: inglês
Generates detailed user flow diagrams in Mermaid syntax from Jira stories or written requirements. Pulls story details via Atlassian MCP, identifies happy paths, error paths, decision points, and system actions. Specializes in clinical trial EDC workflows…
Idioma do texto original: inglês
Analyze user interview transcripts from clinical trial stakeholders (CROs, sponsors, sites) to extract themes, pain points, opportunities, and persona insights.
Idioma do texto original: inglês
Generate authoritative white papers on clinical trial technology topics with research-backed content, references, data visualization concepts, and gate-worthy lead generation value.
Idioma do texto original: inglês
Create compelling customer case studies for Talosix EDC using problem/solution/results format with clinical trial metrics, appropriate anonymization, and approval workflows.
Idioma do texto original: inglês
Assess deal health and risk factors for Talosix EDC opportunities, score deals across multiple dimensions, identify red flags, and recommend actions to improve pipeline forecast accuracy.
Idioma do texto original: inglês
Generates detailed, Figma-ready component specifications from requirements. Produces comprehensive specs covering all states, variants, design token mappings, interaction definitions, responsive behavior, and accessibility requirements. Specializes in…
Idioma do texto original: inglês
Generate conversion-optimized landing page copy for Talosix EDC campaigns with hero sections, feature highlights, CTAs, and social proof tailored to CROs, sponsors, and sites.
Idioma do texto original: inglês
Plan and produce educational webinars for clinical trial audiences including topic selection, speaker preparation, content outlines, promotion strategy, and follow-up sequences.
Idioma do texto original: inglês
Sync test artifacts with Zephyr Scale for the Talosix EDC platform. Map test cases to Jira requirements, generate execution reports, track coverage metrics, and manage test cycles and versions.
Idioma do texto original: inglês
Deep Account-Based Marketing research for Talosix target accounts. Compiles comprehensive account intelligence including clinical trial pipeline, technology landscape, organizational structure, stakeholder mapping, and generates account-specific messaging…
Idioma do texto original: inglês
Prepare for regulatory audits and inspections from FDA, EMA, and sponsors including checklist generation, document review, gap analysis, CAPA preparation, and common findings remediation.
Idioma do texto original: inglês
Manage change control for validated clinical trial systems including impact assessment, classification, documentation requirements, and approval workflows.
Idioma do texto original: inglês
Gather and analyze competitive intelligence on EDC vendors in the clinical trial space. Monitors Medidata Rave, Veeva Vault EDC, Oracle Clinical One, Castor, IQVIA, Signant Health, and others. Produces structured intel reports with strategic implications for…
Idioma do texto original: inglês
Pre-deployment verification checklist for validated clinical trial EDC systems. Covers environment checks, data backup, rollback readiness, validation documentation completeness, and stakeholder notification.
Idioma do texto original: inglês
Create deployment plans for validated GxP environments including validation impact assessment, pre-deployment checklists, deployment steps with rollback criteria, post-deployment verification, and GxP documentation.
Idioma do texto original: inglês