Clinical & Biomedical Specialist – Pharma Consultant (Remote)

About the role

We are partnering with a leading AI lab to engage experienced clinical and biomedical specialists who will help train a cutting‑edge language model on professional documentation, spreadsheets, and slide decks. This remote, part‑time consultancy offers flexible hours and immediate start.

Key responsibilities

• Create, evaluate, and refine AI‑generated clinical study reports, protocol synopses, and regulatory dossier modules.
• Develop and review investigator brochures, medical affairs slide decks, and publication plans.
• Collaborate with AI engineers to improve model performance on pharma‑specific tasks.

Required profile

• 5+ years of experience in clinical research, biomedical science, or pharmaceutical/regulatory affairs.
• Direct experience authoring or reviewing clinical study reports, protocol synopses, or regulatory dossier modules.
• Deep familiarity with ICH‑GCP standards and FDA/EMA regulatory expectations.

Required skills

• Expert‑level document, spreadsheet, and slide craftsmanship.
• Excellent written communication and meticulous attention to detail.

What we offer

• Compensation of $100 per hour.
• Flexible commitment of 5–20 hours per week (or more).
• Fully remote work with autonomy over schedule.