nroze22/TalosixSkills - 第 3 页

job-description

Generate job descriptions for clinical trial technology roles at Talosix. Includes required regulatory knowledge, competitive positioning for the talent market, and DEI-inclusive language.

原文语言：英语

lead-research-assistant

Identify and qualify leads for the Talosix sales team. Finds companies matching target criteria, qualifies them against the ICP, scores them as Hot/Warm/Cool, and produces a prioritized lead list with outreach recommendations for clinical trial EDC sales.

原文语言：英语

linkedin-prospect-research

Research and analyze LinkedIn profiles and companies for Talosix sales targeting. Builds comprehensive prospect dossiers with ICP scoring, buying signals, and personalized talking points for clinical trial EDC sales.

原文语言：英语

meeting-agent

Process meeting notes and transcripts. Extract action items with owners and due dates, create Jira tickets from action items, and generate meeting summaries for distribution.

原文语言：英语

onboarding-checklist

Generate role-customized onboarding checklists for Talosix new hires. Includes GxP training requirements, system access provisioning, 30/60/90 day milestones, and clinical trial domain training.

原文语言：英语

outreach-sequence-generator

Generate personalized multi-touch outreach sequences for Talosix clinical trial EDC sales. Creates 5-7 touch sequences across email and LinkedIn with genuine personalization, consultative tone, and clinical-trial-specific value propositions.

原文语言：英语

policy-document

Draft HR policies and internal documents for Talosix. Ensures compliance with employment regulations, alignment with company culture and values, and uses clear, accessible language.

原文语言：英语

reconcile-payments

Reconcile invoices and payments for Talosix. Flag anomalies and discrepancies, maintain audit trail documentation, and support compliance reporting.

原文语言：英语

regulatory-research

Research and summarize FDA guidance documents, ICH guidelines, 21 CFR Part 11, EU Annex 11, and GDPR for clinical trials with impact analysis on Talosix product features.

原文语言：英语

retrospective

Facilitate sprint and release retrospectives for Talosix teams. Structured format covering what went well, what needs improvement, and action items. Captures learnings and generates improvement actions.

原文语言：英语

risk-assessment

Conduct risk assessments for clinical trial systems using FMEA methodology with risk scoring, mitigation strategies, and acceptance criteria covering patient safety and data integrity.

原文语言：英语

rollback-plan

Create rollback plans for Talosix EDC deployments covering database rollback, code rollback, configuration rollback, data integrity verification, and communication plans.

原文语言：英语

seo-audit

Comprehensive SEO audit for Talosix web properties. Analyzes technical SEO, content SEO, on-page optimization, competitive positioning, and Generative Engine Optimization (GEO). Produces prioritized action items with effort/impact scoring tailored to the…

原文语言：英语

sop-generation

Generate Standard Operating Procedures in GxP compliant format with purpose, scope, responsibilities, procedure steps, references, version control, and approval workflows.

原文语言：英语

talosix-design-system

Talosix design language, component patterns, UX guidelines, design tokens, and Stitch wireframing specifications for the clinical trial EDC platform. Load when generating UI designs, wireframes, user flows, frontend code, or reviewing designs for Talosix.…

原文语言：英语

technical-debt-tracking

Identify, document, prioritize, and track technical debt in Talosix EDC systems. Creates Jira stories, assesses risk in the context of clinical trial regulatory requirements, and monitors debt metrics over time.

原文语言：英语

technical-design

Create technical design documents for Talosix EDC features and systems. Covers architecture, data flow, component design, regulatory compliance, performance, scalability, and security.

原文语言：英语

traceability-matrix

Create requirements traceability matrices mapping user requirements through functional specs, design specs, and test cases with gap analysis in regulatory submission ready format.

原文语言：英语

validation-protocol

Draft validation protocols for clinical trial software including IQ/OQ/PQ, 21 CFR Part 11 compliance, and GAMP 5 risk-based approach with complete test scripts and traceability.

原文语言：英语