nroze22/TalosixSkills - Page 3

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.

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.

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.

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.

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.

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.

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.

reconcile-payments

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

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.

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.

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.

rollback-plan

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

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…

sop-generation

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

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.…

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.

technical-design

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

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.

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.