Medical Writer / Clinical Document Author - praca zdalna

Firma micro1 szuka osoby na stanowisko Medical Writer / Clinical Document Author. Oferta należy do kategorii „Treści i tłumaczenia” i jest w pełni zdalna. Firma nie ogranicza miejsca zamieszkania kandydata, więc zgłoszenie można wysłać z dowolnego miejsca.

Firma podała wynagrodzenie: $50 - $80 za godzinę. Ogłoszenie nie stawia żadnych warunków co do godzin pracy.

Ta oferta przeszła automatyczną kontrolę: na listę nie trafiają ogłoszenia wymagające zagranicznego pozwolenia na pracę, sponsorowania wizy, określonego obywatelstwa ani zamieszkania we wskazanym kraju.

Role Title: Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer’s project focused on developing advanced AI-assisted writing tools for clinical documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required - your domain knowledge is what matters. Scope of Work

* Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.

* Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management.

* Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.

* Trace narrative claims to source records-tables, figures, listings, and protocols-to verify that all assertions are appropriately supported.

* Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.

* Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.

Preferred Qualifications

* Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.

* Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.

* Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.

* Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.

* Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.

* Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.

* Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.

Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents - through your expert input, judgment, and real-world experience. Originally posted on Himalayas