FSP Sr. Clinical Scientist - Immunology

Reposted Yesterday
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Hiring Remotely in Durham, NC, USA
In-Office or Remote
135K-150K Annually
Senior level
Biotech
The Role
Lead Phase 1-3 Clinical Trials, oversee medical monitoring, manage clinical study execution, collaborate on trial designs and protocols, and mentor Clinical Scientists.
Summary Generated by Built In

 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.

Skills Required

  • Degree in Life Sciences or significant experience in clinical development
  • Minimum 2 years pharmaceutical and clinical drug development experience in a Clinical Scientist role
  • Medical monitoring experience
  • TA-specific experience in Immunology
  • Excellent Excel and PowerPoint skills
  • Excellent written and oral communication skills
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The Company
HQ: Research Triangle Park, NC
10,811 Employees

What We Do

Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.

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