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QSP Modeling Intern

unlimited holidays - fully flexible
Remote: 
Full Remote
Contract: 
Experience: 
Entry-level / graduate
Work from: 

Offer summary

Qualifications:

Currently pursuing a PhD or master's degree in pharmaceutical sciences, engineering or related field., Previous QSP modeling experience preferred., Strong data analytics and organizational skills., Excellent verbal and written communication skills., Ability to manage personal workflow effectively..

Key responsabilities:

  • Review, compile, and assemble data for QSP/QST projects.
  • Design, write, test, and maintain biological sub-models using programming.
  • Translate laboratory or clinical data into model parameters.
  • Contribute to the successful completion of the QSP Business Unit’s goals.
  • Prepare reports and presentations for project deliverables.
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Simulations Plus, Inc. SME https://www.simulations-plus.com
51 - 200 Employees
See more Simulations Plus, Inc. offers

Job description

Simulations Plus is a leading developer of modeling and simulation software, and a provider of consulting services. We support our pharmaceutical and biotechnology clients through drug discovery, development research, and regulatory submissions.

 

Maintaining a positive work culture and caring for employee well-being are of utmost importance to the Simulations Plus leadership team. We offer fully remote work, a collaborative work environment, flexible schedules, and more! 

 

The Quantitative Systems Pharmacology (QSP) Modeling Intern will work hand in hand with our amazing QSP modeling team to successfully complete a variety of projects, goals, and analyses. 

 

Business Unit: Quantitative Systems Pharmacology

Department: Scientific 

Internal Grade: 1

Direct Reports: No

Status: Non-Exempt

Location: Remote

 

Job Responsibilities May Include: 

  • Review, compile, and assemble data and related information for one or various critical QSP and/or Quantitative Systems Toxicology (QST) projects
  • Design, write, test, and use computer code to build and maintain the biological sub-model(s) related to a given core area (e.g., QSP models of inflammatory, fibrotic, metabolic, and autoimmune diseases, and immuno-oncology; QST models of liver and kidney safety) and/or general software development
  • Represent compounds in these modeling platforms, including translation of laboratory or clinical data into model parameters
  • Contribute to the activities required for successful completion of the QSP Business Unit’s goals, including those of various internal research and development efforts
  • Combine technical and project management work, including components such as QSP/QST modeling, software code development, and maintenance in Julia, MATLAB, or other designated software environments
  • Prepare reports and presentations and present critical final deliverables for all projects
  • Participate in preparation and review of manuscripts and/or conference abstracts
  • Other duties as assigned 

Qualifications: 

  • Previous QSP modeling or related experience preferred
  • Excellent verbal and written communication skills
  • Strong data analytics and organizational skills
  • Ability to manage personal workflow to meet deadlines
  • Ability to build and maintain positive working relationships 
  • A good team player who meets and exceeds goals
  • Self-motivated, confident, energetic, and creative
  • Ability to maintain client confidentiality 

Education: 

  • Currently working towards a PhD or master’s degree in pharmaceutical sciences, engineering, or related field

 

Find out more about how amazing it is to work at Simulations Plus by visiting www.simulations-plus.com/career-center and apply today!

Required profile

Experience

Level of experience: Entry-level / graduate
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Self-Motivation
  • Creativity
  • Client Confidentiality
  • Teamwork
  • Organizational Skills
  • Verbal Communication Skills

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