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→

US Browse · Boston · Clinical Research Associate

Clinical Research Associate in Boston

Featured Jobs

Daily Net Job Change

−1

Job title

Country

City

Refine

Clinical Trial Monitor Ii - Clinical Trials Office
Dana-Farber Cancer Institute's Center for Global Health
Boston, MA, US
Full time
Base: $74,900.00 - $82,400.00; bonus/equity: not s...
Fully remote
+5y experience
5 years clinical trials experience
3+ years monitoring experience
Bachelor's degree in research compliance
The Clinical Trials Monitor ensures compliance of the clinical research enterprise with federal, state, local, and institutional regulatory policies
5 days ago
Clinical Scientist, Neuroimmunology & Specialty Care, Pdt
Takeda Pharmaceutical Company Limited
Boston, MA, US
Full time
Base: $116,000.00 - $182,270.00; bonus/equity: sho...
Hybrid
Mid-level
5 years clinical development experience
Good clinical practice (gcp) knowledge
Protocol concept and document writing
The role supports the advancement of new therapeutic approaches for people with rare and complex diseases within the Neuroimmunology and Specialty Care team
5 days ago
Sr. Clinical Research Specialist - Site Ops
Iterative Health
Cambridge, NY, United States
On-site
+5y experience
5 years clinical research experience
Phase ii-iv pharmaceutical trials support
Gcp ich fda regulatory knowledge
Iterative Health is a healthcare technology company transforming clinical research through AI and human expertise across a network of 100+ sites
5 days ago
Clinical Research Associate Ii - Oncology (remote Us - Multiple Openings)
AbbVie
Boston, MA, United States
Full time
Not specified; range not disclosed in posting; ben...
Remote
+1y experience
Clinical research monitoring experience
Good clinical practices (gcp) knowledge
Oncology therapeutic area understanding
AbbVie is hiring a Clinical Research Associate II to drive excellence in clinical research and turn science into medicine for patients with serious health issues
10 days ago
Clinical Research Associate
Mass General Brigham
Boston, MA, US
Full time
Base: $20.16 - $29.01phly; bonus/equity: not speci...
Hybrid
+2y experience
Maintain regulatory binders
Submit protocol amendments to irb
Manage adverse event documentation
The position works under general supervision to ensure regulatory requirements for clinical trials are met at Mass General Brigham
12 days ago
Clinical Research Associate
The General Hospital Corporation Mass General Brigham
Boston, MA, US
Full time
Base: $20.16 - $29.01phly; bonus/equity: not speci...
Hybrid
+2y experience
Maintain regulatory binders
Submit protocol amendments to irb
Manage adverse event documentation
The position involves working with clinical teams, Institutional Review Boards, and federal regulatory agencies to ensure compliance
12 days ago
Clinical Research Associate Ii
AbbVie
Boston, MA, United States
Full time
Not specified; short-term incentive programs eligi...
Remote
+1y experience
Good clinical practices gcp compliance
Ich guidelines knowledge
Site evaluation and training
The role serves as the primary point of contact for investigative sites to ensure meaningful partnerships and effective trial conduct
12 days ago
Clinical Scientist, Neuroimmunology & Specialty Care, Pdt
Takeda
Boston, MA, USA
Full time
Base: $116,000.00 - $182,270.00; bonus/equity: sho...
Hybrid
Mid-level
5+ years clinical development experience
Protocol concept and document writing
Regulatory submission preparation
This role supports the advancement of new therapeutic approaches for people with rare and complex diseases within the Neuroimmunology and Specialty Care team
14 days ago
Clinical Scientist, Neuroimmunology & Specialty Care, Pdt
Takeda
Boston, MA, USA
Full time
Base: $116,000.00 - $182,270.00; bonus/equity: sho...
Hybrid
Mid-level
5+ years clinical development experience
Protocol concept and document development
Regulatory submission preparation (ind/nda)
This role supports the advancement of new therapeutic approaches for people with rare and complex diseases within the Neuroimmunology and Specialty Care portfolio
14 days ago
Senior Clinical Lead, Early Clinical & Experimental Therapeutics
Sanofi
Cambridge, MA, US
Full time
Base: $236,250.00 - $341,250.00; bonus/equity: not...
Onsite
Senior
Md or md/phd degree required
3+ years early phase clinical trial experience
Oversight of phase 1/2a oncology trials
This role drives breakthroughs in oncology by developing inhibitors of key signaling pathways as monotherapy or in combination with varied modalities
14 days ago
Clinical Scientist, Neuroimmunology & Specialty Care, Pdt
Takeda
Boston, MA, US
Full time
Base: $116,000.00 - $182,270.00; bonus/equity: sho...
Hybrid
Mid-level
5+ years clinical development experience
Protocol concept and document development
Regulatory submission preparation (ind/nda)
This role supports the advancement of new therapeutic approaches for people with rare and complex diseases within the Neuroimmunology and Specialty Care team
14 days ago
Senior Clinical Lead, Early Clinical & Experimental Therapeutics
Sanofi
Cambridge, MA, US
Full time
Base: $236,250.00 - $341,250.00; bonus/equity: not...
Onsite
Senior
Md or md/phd degree required
3+ years early phase clinical trial experience
Oversight of phase 1/2a oncology studies
This role drives breakthroughs in oncology by developing inhibitors of key signaling pathways as monotherapy or in combination with other agents
15 days ago
Clinical Research Associate
621
Boston, MA, US
Full time
Base: $20.16 - $29.01phly; bonus/equity: not speci...
Hybrid
+2y experience
Maintain study-specific regulatory binders
Submit protocol amendments to irb
Manage adverse event documentation
The position involves working with clinical teams, Institutional Review Boards (IRB), sponsors, and federal regulatory agencies to ensure compliance
15 days ago
Senior Clinical Lead, Early Clinical & Experimental Therapeutics
Sanofi Consumer Healthcare
Cambridge, MA, US
Full time
Base: $236,250.00 - $341,250.00; bonus/equity: not...
Onsite
Senior
M.d. or m.d./ph.d. degree required
3+ years early phase clinical trial experience
Oversight of phase 1/2a oncology trials
This role drives breakthroughs in oncology by developing inhibitors of key signaling pathways as monotherapy or in combination with varied modalities
16 days ago
Clinical Program Lead (cpl) - Rlt Focus
Novartis
Cambridge, MA, USA
Full time
Base: $248,500.00 - $461,500.00 usd annual; bonus/...
Hybrid
+2y experience
Md or do degree required
Board-certification in oncology specialty
2 years pharmaceutical industry experience
The role provides strategic medical guidance and leads the development of experimental oncology agents within the TCO portfolio
16 days ago
Clinical Research Associate
Center for Integration Science
Boston, MA, US
Full time
Base: $20.16 - $29.01phly; bonus/equity: not speci...
Hybrid
+2y experience
Maintain study-specific regulatory binders
Submit protocol amendments to irb
Manage adverse event documentation
The position involves ensuring regulatory requirements for clinical trials are met through collaboration with IRBs, sponsors, and federal agencies
16 days ago
Manager, Clinical Data Management
CRISPR Therapeutics
Boston, Massachusetts, United States
Full time
Base: $123,000 to $133,000; bonus/equity: included...
Fully remote
+7y experience
7+ years clinical data management experience
Medidata rave edc proficiency
Cdash/sdtm/cdisc standards knowledge
The Manager of Clinical Data Management will lead clinical data management activities across all stages of clinical development for CRISPR Therapeutics
17 days ago
Manager, Clinical Data Management
CRISPR Therapeutics
Boston, Massachusetts, United States
Full time
Base: $123,000 to $133,000; bonus/equity: included...
Fully remote
+7y experience
7+ years clinical data management experience
Medidata rave edc database proficiency
Cdash/sdtm/cdisc standards knowledge
The Manager of Clinical Data Management will lead clinical data management activities across all stages of clinical development for CRISPR Therapeutics
17 days ago
Clinical Trial Manager
TransMedics
Somerville, MA, US
Full time
Base: $112,400.00 – $140,200.00; bonus/equity: eli...
+7y experience
7+ years cra or cta experience
Medical device industry background
Gcp ich fda regulatory knowledge
This role leads the end-to-end execution of clinical trials ensuring studies are delivered on time, within budget, and in compliance with regulatory standards
17 days ago
Senior Clinical Lead, Early Clinical & Experimental Therapeutics
Sanofi Genzyme
Cambridge, MA, US
Full time
Base: $236,250.00 - $341,250.00; bonus/equity: not...
Onsite
Senior
M.d. or m.d./ph.d. degree required
3+ years early phase clinical trial experience
Design and execution of phase 1/2a studies
This role drives breakthroughs in oncology by developing inhibitors of key signaling pathways as monotherapy or in combination
17 days ago
Clinical Scientist, Neuroimmunology & Specialty Care, Pdt
Takeda UK
Boston, MA, US
Full time
Base: $116,000.00 - $182,270.00; bonus/equity: sho...
Hybrid
Mid-level
5 years clinical development experience
Good clinical practice (gcp) knowledge
Protocol concept and document writing
This role supports the advancement of new therapeutic approaches for people with rare and complex diseases within the Neuroimmunology and Specialty Care team
17 days ago
Clinical Scientist, Neuroimmunology & Specialty Care, Pdt
Takeda
Boston, MA, US
Full time
Base: $116,000.00 - $182,270.00; bonus/equity: sho...
Hybrid
Mid-level
5+ years clinical development experience
Protocol concept and document development
Regulatory submission preparation (ind/nda)
This role supports the advancement of new therapeutic approaches for people with rare and complex diseases within the Neuroimmunology and Specialty Care team
17 days ago
Senior Clinical Research Director, I&i
Sanofi
Cambridge, MA, US
Full time
Base: $236,250.00 - $393,750.00; bonus/equity: not...
Onsite
Medical expertise in clinical studies
Late stage clinical development experience
Protocol and study document leadership
The role serves as a mentor for other Clinical Research Directors and Clinical Scientists while driving breakthrough immunoscience research
17 days ago
Senior Clinical Lead, Early Clinical & Experimental Therapeutics
Sanofi UK
Cambridge, MA, United States
Full time
Base: $236,250.00 - $341,250.00; bonus/equity: not...
Onsite
Senior
Md or md/phd degree required
3+ years early phase clinical trial experience
Oversight of phase 1/2a oncology studies
This role drives breakthroughs in oncology by developing inhibitors of key signaling pathways as monotherapy or in combination with varied modalities
17 days ago
Senior Clinical Lead, Early Clinical & Experimental Therapeutics
Sanofi
Cambridge, MA, US
Full time
Base: $236,250.00 - $341,250.00; bonus/equity: not...
Onsite
Senior
Md or md/phd degree required
3+ years early phase clinical trial experience
Oversight of phase 1/2a oncology trials
This role drives breakthroughs in oncology by developing inhibitors for key signaling pathways as monotherapy or in combination therapies
17 days ago

Subscribe to fresh job alerts

Clinical Research Associate in Boston

Clinical Trial Monitor Ii - Clinical Trials Office

Clinical Scientist, Neuroimmunology & Specialty Care, Pdt

Sr. Clinical Research Specialist - Site Ops

Clinical Research Associate Ii - Oncology (remote Us - Multiple Openings)