Kyverna Therapeutics seeks a Contract Safety Writer/Scientist in Pharmacovigilance to prepare high-quality safety documentation and responses to FDA inquiries. Remote-eligible with a 6+ month engagement and part-time hours.
The role emphasizes translating complex safety data into regulatory-compliant documents and coordinating with cross-functional teams to support regulatory submissions and safety reviews.
#J-18808-LjbffrRemote Safety Writer – Pharmacovigilance (Contract) in Location not specified at Unknown Company
This position is listed as part time and able to be worked remotely.