Clinical & Biomedical Specialist / Pharma Consultant

Ethos

United States

À distance

USD 23 000 - 91 000

Temps partiel

Il y a 6 jours
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Avantages offerts par ce poste

Health insurance

Résumé du poste

Ethos is seeking experienced clinical and biomedical specialists to help train an AI language model on professional documents, spreadsheets, and slide decks across core workflows.

This fully remote engagement offers flexible hours (5–20 per week) at $100/hour, with potential for more. Candidates should have 5+ years in clinical research, regulatory affairs, or biomedical science and strong document craftsmanship with attention to detail.

Qualifications

  • Direct experience authoring or reviewing clinical study reports, protocol synopses, or regulatory dossier modules for a pharmaceutical, biotech, or CRO organization
  • Deep familiarity with ICH-GCP standards, FDA/EMA regulatory expectations, and the scientific rigor required in investigator brochures and medical affairs materials
  • Expert-level document, spreadsheet, and slide craftsmanship, with excellent written communication and attention to detail

Responsabilités

  • 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.
  • Collaborate with subject-matter experts to ensure accuracy and regulatory compliance of produced materials
  • Maintain high quality and consistency across all AI-assisted documents, spreadsheets, and decks

Connaissances

Written communication
Attention to detail
Regulatory affairs knowledge
ICH-GCP familiarity

Formation

5+ years in clinical research, biomedical science, or pharmaceutical/regulatory affairs

Description du poste

Pay: $100/hr, up to $2.0k/week

We're working with a leading foundational AI lab to find experienced clinical and biomedical specialists who can help train their latest language model on professional document, spreadsheet, and slide deck tasks.We're looking for pharma and clinical development professionals 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.
Compensation: $100/hour
Commitment: Flexible, 5-20 hours per week (or more if desired)
Location: Fully remote, work on your own schedule
Start date: ASAP
Qualifications:

  • Direct experience authoring or reviewing clinical study reports, protocol synopses, or regulatory dossier modules for a pharmaceutical, biotech, or CRO organization
  • Deep familiarity with ICH-GCP standards, FDA/EMA regulatory expectations, and the scientific rigor required in investigator brochures and medical affairs materials
  • Expert-level document, spreadsheet, and slide craftsmanship, with excellent written communication and attention to detail
About Ethos

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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