Negotiable
Outside
Remote
sacramento, california (remote)
Summary: The role of Clinical Safety Scientist involves leading program-level safety data review for a large Phase III program at a biotech company. This part-time, remote position requires a seasoned professional with an advanced degree. The contract is through 12/31/25, with the possibility of extension. The role does not involve pharmacovigilance operations such as ICSR processing or vendor management.
Key Responsibilities:
- Lead program-level safety data review for a large Phase III program.
- Ensure compliance with safety data management protocols.
- Collaborate with cross-functional teams to assess safety data.
- Provide expert guidance on safety data interpretation.
Key Skills:
- Advanced degree (PhD, PharmD, or MD) required.
- Experience in clinical safety and data review.
- Strong analytical and communication skills.
- Ability to work independently in a remote setting.
Salary (Rate): £100 per hour
City: Sacramento
Country: United States
Working Arrangements: remote
IR35 Status: outside IR35
Seniority Level: Mid-Level
Industry: Other
description: job summary: Contract through 12/31/25 (extension possible) Part-Time/Flex (~20 hrs/week) REMOTE | W2 or 1099 | Can submit above published rate Seeking a seasoned Clinical Safety Scientist to lead program-level safety data review for a large Phase III program at a biotech company. Note: This is not a PV Ops role (no ICSR processing, signal detection, aggregate reporting, vendor management) MUST HAVES Advanced degree required (PhD, PharmD, or MD prefer
title: clinical safety scientist (program-level data review)
salary: $100 per hour
location: sacramento, california (remote)
misc1: Outside IR35
misc2: