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FSP Clinical Scientist III / Medical Science Liaison

Fortrea•United Kingdom•🌍 Remote
Full-timeSenior
$130k - $190k
per year
👁️ 0 views•📝 0 applications•Posted 9/21/2026•Expires 11/20/2026
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Job Description

FSP Clinical Scientist III / Medical Science Liaison – US Remote based Fortrea is hiring a Medical Science Liaison (MSL) – FSP to provide ongoing in-depth analysis and scientific input into development and execution of protocols and clinical development plans by working with the medical/scientific/regulatory team to creatively solve a wide range of medical/scientific/clinical/regulatory problems.

Key / Core Responsibilities You will serve as a resource for the Medical Monitor by tracking and reviewing ongoing study specific safety data (e. g. , adverse events, vitals, ECGs, and safety lab results) to identify safety trends.

You will act as a liaison between the Medical Monitor in all communications between study sites, Fortrea project staff and Sponsors regarding protocol or other study-related questions, including documenting, tracking, and follow-up on all issues.

You will review and evaluate CPS proposals and provide clinical and scientific support, as needed. This includes drafting study outlines/designs and providing guidance on early clinical development strategies.

You will provide ongoing in-depth analysis and scientific input into development and execution of protocols and clinical development plans. You will work with the medical/scientific/regulatory team to creatively solve a wide range of medical/scientific/clinical/regulatory problems.

You will establish and maintain close affiliations with the Fortrea and larger scientific community. You will provide scientific and logistical rationale/input for including biomarkers or other lab markers in Proof-of-Concept (POC) studies. You will attend Kick-off Meetings and SIVs/Investigator Meetings.

Supports training in key medical/scientific areas. You will attend Team Meetings. Ensure that any medical/safety issues discussed at the meeting are resolved by the medical monitor in a timely manner.

You will support CPS Medical Monitors in tracking and documenting any Inclusion/Exclusion criteria or protocol-related que

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