Position: Quality Control Medical Writing
Location: Hybrid in San Francisco CA (4-5 days in office Mon-Sat)
Duration: Fulltime
Year of Experience - 3
Scope of Role
- Helping design AI systems that write regulatory documents.
- Deconstructing authoring/review/QC heuristics for engineers.
- Evaluating AI-generated content quality and identifying edge cases.
- Bridging the gap between domain expertise (medical writing) and technical product development.
MUST HAVE SKILLS
Must Have Skills for Role:
- candidates MUST have atleast 3 years of US-based experience in the US (working remotely for a US company in India/etc. does not count)
- Additionally if applicable please explicitly state that the candidate is open to immediate relocation since these are IN-OFFICE in SF positions.
3 years of medical writing experience in regulatory affairs.
Direct experience with CTD documents (non-clinical and CMC).
Knowledge of FDA EMA and ICH guidelines.
Ability to extract and document rules/logic for technical teams.
Strong QC capabilities.
Nice to Have Skills for Role:
Familiarity with structured content formats like XML or JSON.
Experience working with life sciences software tools.
Position: Quality Control Medical Writing Location: Hybrid in San Francisco CA (4-5 days in office Mon-Sat) Duration: Fulltime Year of Experience - 3 Scope of Role Helping design AI systems that write regulatory documents. Deconstructing authoring/review/QC heuristics for engineers. Evaluatin...
Position: Quality Control Medical Writing
Location: Hybrid in San Francisco CA (4-5 days in office Mon-Sat)
Duration: Fulltime
Year of Experience - 3
Scope of Role
- Helping design AI systems that write regulatory documents.
- Deconstructing authoring/review/QC heuristics for engineers.
- Evaluating AI-generated content quality and identifying edge cases.
- Bridging the gap between domain expertise (medical writing) and technical product development.
MUST HAVE SKILLS
Must Have Skills for Role:
- candidates MUST have atleast 3 years of US-based experience in the US (working remotely for a US company in India/etc. does not count)
- Additionally if applicable please explicitly state that the candidate is open to immediate relocation since these are IN-OFFICE in SF positions.
3 years of medical writing experience in regulatory affairs.
Direct experience with CTD documents (non-clinical and CMC).
Knowledge of FDA EMA and ICH guidelines.
Ability to extract and document rules/logic for technical teams.
Strong QC capabilities.
Nice to Have Skills for Role:
Familiarity with structured content formats like XML or JSON.
Experience working with life sciences software tools.
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