FSP Clinical Scientist III / Medical Science Liaison

Fortrea

. Provide ongoing in-depth analysis and scientific input into development and execution of protocols and clinical development plans .

Posted 9/18/2026full-timeRemote • United StatesSeniorLead💰 $130,000 - $190,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical development and medical monitoring, with a strong focus on Hereditary Angioedema (HAE) and adherence to GCPs and regulatory guidelines. Proven ability to analyze safety data, support clinical protocols, and collaborate effectively with medical and scientific teams.

Highest-signal resume keywords

Doctor Of Medicine (MD)Clinical Practice ExperienceHereditary Angioedema (HAE) ExpertiseMedical MonitoringGCP Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data InterpretationClinical Development PlanningProtocol DevelopmentSafety Data ReviewBiomarker Analysis

Soft Skills

CollaborationCommunicationProblem Solving

Industry Keywords

Pharmaceutical ResearchClinical ResearchCRO ExperienceRegulatory Agency GuidelinesInclusion/Exclusion Criteria

About the role

Key responsibilities & impact

Provide ongoing in-depth analysis and scientific input into development and execution of protocols and clinical development plans
Work with the medical/scientific/regulatory team to solve medical, scientific, clinical, and regulatory problems
Serve as a resource for the Medical Monitor by tracking and reviewing study-specific safety data to identify safety trends
Act as liaison among the Medical Monitor, study sites, Fortrea project staff, and Sponsors regarding protocol and study-related questions
Document, track, and follow up on study-related issues
Review and evaluate CPS proposals and provide clinical and scientific support
Draft study outlines and designs and provide guidance on early clinical development strategies
Establish and maintain affiliations with the Fortrea and larger scientific community
Provide rationale and input for including biomarkers or other lab markers in Proof-of-Concept studies
Attend Kick-off Meetings, SIVs/Investigator Meetings, and Team Meetings
Support training in key medical/scientific areas
Ensure medical and safety issues discussed in team meetings are resolved by the Medical Monitor
Support CPS Medical Monitors in tracking and documenting Inclusion/Exclusion criteria and protocol-related questions and answers
Perform other related duties as assigned

Requirements

What you’ll need

Doctor of Medicine (MD) degree required
Prior hands-on experience as licensed physician (MD) in clinical practice
2+ years prior hands-on experience as a licensed physician in clinical practice preferred
TA-specific experience in Hereditary Angioedema (HAE) is required
Progressive responsibility within CRO or Sponsor environment
Knowledge of GCPs and regulatory agency guidelines
Ability to conduct limited review of related literature and references and apply the information
Skilled in data interpretation
English speaking, writing, and reading
Minimum 10+ years pharmaceutical and clinical research experience, including at least 5+ years in a medical monitoring/medical data review role
Heavy travel required throughout the year
Must be authorized to work in the United States on a full-time basis
Company does not provide visa sponsorship now or in the future

Benefits

Comp & perks

Medical insurance
Dental insurance
Vision insurance
Life insurance
Short-term disability (STD)
Long-term disability (LTD)
401(K)
Paid time off (PTO) or Flexible time off (FTO)
Company bonus where applicable