# Safety Writer/Scientist – Contract at Kyverna Therapeutics

- Company: Kyverna Therapeutics
- What the company does: KYVERNA is pioneering a new class of treatments and potential cures for serious autoimmune diseases. Backed by Insight Partners.
- Company website: https://kyvernatx.com
- Type: Startups
- Level: Mid level
- Location: Remote
- Work setup: Remote
- Posted: 2026-09-18
- Apply by: 2026-11-02
- Apply: https://jobs.lever.co/Kyverna/81061bf8-427d-4472-8729-0c2dddc32cf9
- Page: https://www.1752.vc/careers/jobs/kyverna-therapeutics-safety-writer-scientist-contract/

## About the role

Kyverna is seeking a Contract Safety Writer/Scientist – Pharmacovigilance (Consultant) with deep expertise in Safety/Pharmacovigilance to support critical regulatory and medical safety documentation activities. This individual will play a key role in preparing high-quality safety regulatory documents, such as drafting responses to FDA clinical or postmarket Information Requests (IRs), supporting external advisory committee meetings, safety related clinical and medical inquiries, etc.

## What they're looking for

- Advanced degree in life sciences, pharmacy, nursing, public health, or related scientific field (doctorate level preferred)
- 8+ years of medical writing/safety scientist experience, with significant focus in safety, clinical, or regulatory documents
- Experience with writing safety signal assessment documents
- Prior experience with writing and preparation for FDA advisory committees is highly valued
- Demonstrated experience drafting responses to FDA Information Requests related to safety
- Strong understanding of pharmacovigilance principles, including adverse event reporting, signal detection, and risk management

Tags: Drug Safety/Pharmacovigilance