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FSP Sr. Clinical Scientist - Immunology
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Fortrea

FSP Sr. Clinical Scientist - Immunology

Toronto, ON, Canada

Target Pay Range for US: $135-150K · Full-time

Within 25 km of Richmond Hill · About 19.1 km from the city centre

Apply on careers.fortrea.com About employer

Applications open in a new tab.

Job details

Pay: Target Pay Range for US: $135-150K
Job type: Full-time
Posted: Sep 22, 2026

Original job description

Senior Clinical Scientist, FSP – Immunology – Remote US or Canada 

***Position leads Phase 1-3 Clinical Trials and oversees medical monitoring.   

This is not a laboratory/research scientist role.*** 

In this role, the selected candidate will lead/support studies; be accountable for the clinical/scientific execution of the protocol; be the clinical point of contact for scientific issues/questions for internal and external stakeholders (e.g., IRB, sites); and act as scientific lead on Clinical Trial Team (CTT).

Responsibilities include:

Responsible for trial design and endpoint development in collaboration with CD; collaborates with medical writing to develop trial results communication for investigators

Leads the Medical Monitoring (MM) team in performing MM activities, including development of the Medical Monitoring Plan (MMP) and review of SAE reports, monitoring data issues and central lab reports

Sets up/supports SAC, DMC, adjudication committee; provides scientific input to SM for data management activities (e.g. EDC, DRP, CRF’s_

Protocols/amendments – collaborates with medical writing, participates in governance committee review; authors protocol clarification letters; reconciles and reviews all protocol deviation classifications and assess and prepares protocol deviation list for the CSR

May act as mentor to other Clinical Scientists

Requirements:

Education:

Degree in Life Sciences or significant experience in clinical development (>14 years)

BS/BA with 7+ yrs clinical research experience

MS/PhD with 5+ years clinical research experience

Experience:

Minimum 2 years pharmaceutical and clinical drug development experience in a Clinical Scientist role as a lead required.

Proven ability to effectively manage multiple complex studies

Medical monitoring experience required

TA-specific experience in Immunology

Excellent Excel and PP skills required

Excellent written and oral communication skills

Target Pay Range for US: $135-150K

Physical Demands/Work Environment:

Work Environment:

Work is performed in an office environment with exposure to electrical office equipment.
Frequent travel to clients/ site locations with occasional travel both domestic and international.

Physical Requirements:

Ability to sit for extended periods and operate a vehicle safely.
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Regular and consistent attendance.
Varied hours may be required.

Learn more about our EEO & Accommodations request here.

Apply on careers.fortrea.com About employer

More about this job

Responsibilities

The Senior Clinical Scientist at Fortrea will design trials, develop endpoints, and lead medical monitoring for immunology studies. They will also answer scientific questions for sponsors, IRBs and sites, and may mentor other clinical scientists.

Requirements

Fortrea asks for a life sciences degree or extensive clinical development experience, at least 2 years as a lead Clinical Scientist, and medical monitoring experience. Candidates also need immunology experience, strong Excel and PowerPoint skills, and excellent written and oral communication.

Skills

Clinical trial design
Endpoint development
Medical monitoring
Medical Monitoring Plan development
SAE review
Protocol authoring
Protocol deviation management
Clinical study report
Data monitoring committee support
Electronic data capture
Case report forms
Microsoft Excel
Microsoft PowerPoint
Immunology
Clinical development
Regulatory communication
Stakeholder management
Mentoring

Keywords

Clinical Scientist
Clinical Trials
Phase 1
Phase 2
Phase 3
Immunology
Medical Monitoring
Medical Monitoring Plan
Protocol Development
Protocol Deviations
Clinical Study Report
Endpoint Development
Clinical Data Management
Electronic Data Capture
Excel
PowerPoint
Clinical Development
Pharmaceutical
FSP
Remote

Tools

Excel
EDC
CRF

Languages

English

Seniority

Senior

Fields of study

Life Sciences

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