FSP Sr. Clinical Scientist - Immunology

Fortrea

$135K — $150K *
US-Anywhere
+ 2 other locationsRemote
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Degree in Life Sciences or >14 years of clinical development experience
  • BS/BA with 7+ years clinical research experience
  • MS/PhD with 5+ years clinical research experience
  • Minimum 2 years in pharmaceutical/clinical drug development in a lead role
  • Medical monitoring experience is mandatory
  • Experience in Immunology therapeutic area is essential
  • Proficiency in Excel and PowerPoint, with strong communication skills

Responsibilities

  • Lead the design and development of clinical trial protocols and endpoints with cross-functional teams
  • Oversee and direct Medical Monitoring team activities, ensuring adherence to protocols
  • Establish scientific input for data management and coordinate committee setups
  • Collaborate on protocol authorship and governance, including clarification letters
  • Mentor and guide junior Clinical Scientists

Benefits

  • Remote work flexibility in the US or Canada
  • Opportunity to lead significant clinical trials
  • Engagement with cross-functional stakeholders
  • Professional development through mentorship
  • Collaboration with knowledgeable teams in the Immunology field
Full 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.


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