Expert Opportunity - Clinical Research Associate ($100/Hr, Up To $2,000/Week) (New South Wales)

Expert Opportunity - Clinical Research Associate ($100/Hr, Up To $2,000/Week) (New South Wales)

22 Sep
|
Ethos
|
New South Wales

22 Sep

Ethos

New South Wales

Job Description
About This Prospect
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We're working with a leading foundational AI lab to find experienced clinical research associates who can help train their latest language model on professional document, spreadsheet, and slide deck tasks.
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About This Opportunity
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We're working with a leading foundational AI lab to find experienced clinical research associates who can help train their latest language model on professional document, spreadsheet, and slide deck tasks.
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We're looking for clinical research associates with 5+ years in clinical research, biomedical science, or
pharmaceutical/regulatory
affairs to create, evaluate, and refine AI-generated documents, spreadsheets, and slide decks across core workflows: clinical study reports, protocol synopses, investigator brochures, regulatory dossier modules, medical affairs slide decks, and publication plans.
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Compensation: $100/hour
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Commitment: Flexible, 5-20 hours per week (or more if desired)
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Location: Fully remote, work on your own schedule
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Start date: ASAP
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Qualifications
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Direct experience authoring or reviewing clinical study reports, protocol synopses, or regulatory dossier modules for a pharmaceutical, biotech,



or CRO organization
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Deep familiarity with ICH-GCP standards, FDA/EMA regulatory expectations, and the scientific rigor required in investigator brochures and medical affairs materials
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Expert-level document, spreadsheet, and slide craftsmanship, with excellent written communication and attention to detail
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About Ethos
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Ethos is a new expert network built by a
McKinsey/SoftBank/DeepMind
team and backed by world-leading investors like General Catalyst. We connect experts with investors and consultancies for paid expert calls, speaking engagements, and advisory opportunities.
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Key Requirements
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Direct experience authoring or reviewing clinical study reports, protocol synopses, or regulatory dossier modules for a pharmaceutical, biotech, or CRO organization
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Deep familiarity with ICH-GCP standards, FDA/EMA regulatory expectations, and the scientific rigor required in investigator brochures and medical affairs materials
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Expert-level document, spreadsheet, and slide craftsmanship, with excellent written communication and attention to detail
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📌 Expert Opportunity - Clinical Research Associate ($100/Hr, Up To $2,000/Week) (New South Wales)
🏢 Ethos
📍 New South Wales

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