Quality Control Medical Writing Job at Serene Healthcare Staffing in San Francis
Serene Healthcare Staffing, San Francisco, CA, United States
Full time | Serene Healthcare Staffing | United States
Posted On 04/01/2026
Job Information Pharma/Biotech/Clinical Research
Work Experience 4-5 years
City San Francisco
State/Province California
94102
Job Description 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.
Requirements Must Have Skills for Role:
candidates MUST have at least 3 years of US-based experience in the US.
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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Posted On 04/01/2026
Job Information Pharma/Biotech/Clinical Research
Work Experience 4-5 years
City San Francisco
State/Province California
94102
Job Description 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.
Requirements Must Have Skills for Role:
candidates MUST have at least 3 years of US-based experience in the US.
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.
#J-18808-Ljbffr