Workopia is a free MCP server that provides AI-powered job search, resume building, and career advice. It works with Claude Desktop, ChatGPT, OpenClaw, Cursor, and any MCP-compatible AI assistant. Jobs are sourced directly from employer career pages, not scraped from job boards.

How do I add Workopia to Claude Desktop?

Open Claude Desktop, go to Settings, then MCP Servers, and click Add Server. Enter the URL: https://workopia.io/api/mcp-gpt. No API key is needed. You can then search jobs, build resumes, and get career advice directly in your Claude conversations.

Yes, Workopia is completely free to use. No subscription, no payment, and no login required. Job search and career advice are unlimited. Resume generation is rate-limited to 20 per hour per user to prevent abuse.

Where does Workopia get its job data?

Workopia sources jobs directly from employer career pages and ATS feeds such as Lever. It does not scrape LinkedIn, Indeed, SEEK, or other job boards. Every job listing links to the official employer posting.

Does Workopia store my resume?

No. Resume content submitted via MCP is processed in-memory for PDF generation and discarded after the response. No copies are saved server-side. Workopia does not store conversation history, personal information, or user identity from MCP interactions.

What AI platforms does Workopia work with?

Workopia works with any MCP-compatible AI client, including Claude Desktop, Claude Code, ChatGPT, OpenClaw (which supports Slack, Discord, WhatsApp, Telegram, and more), Cursor, Windsurf, and JetBrains IDEs. Just add the endpoint URL: https://workopia.io/api/mcp-gpt.

NEWWorkopia Intelligence is now in beta→

Ireland Browse · Little Island · Other - Healthcare

Other - Healthcare in Little Island

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Associate/sr. Associate - Trial Capabilities - Budgets & Contracts - German
Eli Lilly
Little Island, Ireland
Full time
Not specified; not specified; benefits include hea...
Hybrid
Budget and contract negotiation skills
German and english language fluency
Clinical research experience required
The role provides clinical trial capabilities to ensure investigator sites meet enrollment requirements from a budget and contracts perspective
44 days ago
Expert Specialist - Global Scientific Communications - Regulatory
Eli Lilly
Little Island, Ireland
Full time
Not specified; not specified; benefits include hea...
Hybrid
+1y experience
1 year clinical research or pharmaceutical experience
Word processing and spreadsheet formatting skills
Editing experience with english grammar command
The role supports the delivery of Global Scientific Communications regulatory documents through planning, tracking, and compliance activities
44 days ago
Expert Specialist - Clinical Development
Eli Lilly
Little Island, Ireland
Full time
**
+2y experience
Two-year degree or 2 years administrative experience
Proficiency in microsoft word excel powerpoint project
Experience with clinical trial database systems
The Expert Specialist provides technical and project administrative support to Clinical Development Trial Leads to enable on-time and on-budget delivery of key tasks
44 days ago
Associate/sr. Associate - Trial Capabilities - Budgets & Contracts - German
Eli Lilly UK
Little Island, Ireland
Full time
Not specified; not specified; benefits include hea...
**
German language proficiency
English language proficiency
Budget and contract negotiation
The role provides clinical trial capabilities to ensure investigator sites meet requirements for enrolling study participants from budgets and contracts perspectives
48 days ago
Associate/sr Associate/ Manager/sr Manager/, Gra-emea Regional Regulatory Clinical Trial Submission Lead
Eli Lilly
Little Island, Ireland
Full time
Hybrid
+3y experience
Bachelor's degree in scientific or health sciences
Fluency in english language
Knowledge of eu clinical trial regulations
The role is accountable for establishing local regulatory strategy and plans for assigned clinical trials across the European Union region
48 days ago
Expert Specialist - Global Scientific Communications - Regulatory
Eli Lilly UK
Little Island, Ireland
Full time
Not specified; not specified; benefits include hea...
Hybrid
+1y experience
1 year clinical research experience
1 year editing and proofreading skills
Word processing and spreadsheet management
The role supports the delivery of Global Scientific Communications regulatory documents through comprehensive planning, tracking, and compliance management
48 days ago
Associate/sr Associate/ Manager/sr Manager/, Gra-emea Regional Regulatory Clinical Trial Submission Lead
Eli Lilly
Little Island, Ireland
Full time
Not specified; not specified; benefits include hea...
Hybrid
+3y experience
Bachelor's degree in scientific or health sciences
Fluency in english language
Knowledge of eu clinical trial regulations
The role is accountable for establishing local regulatory strategy and plans for assigned clinical trials across the European Union region
52 days ago
Expert Specialist - Global Scientific Communications - Regulatory
Eli Lilly
Little Island, Ireland
Full time
Not specified; not specified; benefits include hea...
Hybrid
+1y experience
1 year clinical research or pharmaceutical experience
Word processing and spreadsheet management skills
Editing and proofreading expertise with english grammar
The role supports the delivery of Global Scientific Communications regulatory documents through comprehensive planning, tracking, and compliance activities
52 days ago
Associate/sr Associate/ Manager/sr Manager/, Gra-emea Regional Regulatory Clinical Trial Submission Lead
Eli Lilly
Little Island, Ireland
Full time
Not specified; not specified; comprehensive benefi...
Hybrid
+3y experience
Bachelor's degree in scientific or health sciences
Fluency in english language
Knowledge of eu clinical trial regulations
The role is accountable for establishing local regulatory strategy and plans for assigned clinical trials across the European Union region
52 days ago
Associate / Senior Associate - Trial Capabilities - Spanish Speaking
Eli Lilly
Little Island, Ireland
Full time
Not specified; not specified; benefits include hea...
Hybrid
Senior
Spanish language proficiency required
Bachelor's degree in scientific field
Two years clinical research experience
The role involves initiating investigator site activities including the collection of regulatory documents and negotiation of informed consent forms
52 days ago
Associate Director/director, Gra-cmcd Diagnostics Regulatory Scientist - Ivd Studies And Clinical Trial Support
Lilly
Little Island, Ireland
Full time
Not specified; not specified; benefits include hea...
Hybrid
Eu ivdr regulatory knowledge
Ivd performance study execution
Clinical trial application support
The role is accountable for assessing, establishing, and operationalizing the regulatory strategy for IVD performance studies and clinical trials using IVDs
52 days ago
Expert Specialist - Global Scientific Communications - Regulatory
Eli Lilly
Little Island, Ireland
Full time
Not specified; not specified; benefits include hea...
Hybrid
+1y experience
1 year clinical research experience
1 year editing and proofreading skills
Document control and workflow systems knowledge
The role supports the delivery of Global Scientific Communications regulatory documents through comprehensive planning, tracking, and compliance activities
52 days ago

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Other - Healthcare in Little Island

Associate/sr. Associate - Trial Capabilities - Budgets & Contracts - German

Expert Specialist - Global Scientific Communications - Regulatory

Expert Specialist - Clinical Development

Associate/sr. Associate - Trial Capabilities - Budgets & Contracts - German

Associate/sr Associate/ Manager/sr Manager/, Gra-emea Regional Regulatory Clinical Trial Submission Lead

Expert Specialist - Global Scientific Communications - Regulatory

Associate/sr Associate/ Manager/sr Manager/, Gra-emea Regional Regulatory Clinical Trial Submission Lead

Expert Specialist - Global Scientific Communications - Regulatory

Associate/sr Associate/ Manager/sr Manager/, Gra-emea Regional Regulatory Clinical Trial Submission Lead

Associate / Senior Associate - Trial Capabilities - Spanish Speaking

Associate Director/director, Gra-cmcd Diagnostics Regulatory Scientist - Ivd Studies And Clinical Trial Support

Expert Specialist - Global Scientific Communications - Regulatory