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Fortrea via Workday

FSP Sr. Clinical Scientist - Immunology

CanadaUnited States senior
still open verified 6h ago posted 10d ago seen just now
Apply at fortrea.wd1.myworkdayjobs.com

This is the employer's own posting, not a copy on a job board.

What we know

Is it still open?

Confirmed still open

Last checked 6h ago — checked against the employer's own applicant tracking system, which is the company answering directly.

We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.

Check this listing's status as JSON

How old is it?

Posted 10d ago

The date the source published, not the day we noticed it (2026-09-21). Last seen at its source just now.

We have tracked this listing since 22 Sep 2026 (9 days). The employer's own board has carried it every time we have read it, most recently just now.

Is it remote?

The listing says yes

The location field doesn't say remote, so our assessment is based on the title or the description. Read the listing before applying.

Who may apply?

Canada, United States

The description states no restriction of its own. This is the source's own tag.

Pay not stated

Similar roles pay $100k–140k/yr

Middle 50% of 13 listings that do state pay — Healthcare · all levels · Canada · USD/year. This employer has published no salary; this is what comparable listings we hold disclose, never converted between currencies or periods. How this is calculated.

Carried by 1 source

The listing

 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 at fortrea.wd1.myworkdayjobs.com