Demo

Senior Principal Research Scientist

Randstad Life Sciences US
North Chicago, IL Contractor
POSTED ON 4/18/2025
AVAILABLE BEFORE 5/8/2025
Job Summary

Are you a seasoned biomedical professional passionate about advancing drug delivery to the brain? A leading biopharmaceutical company in North Chicago, IL is seeking a Sr. Principal Research Scientist - Preclinical Project Manager to lead the investigation of innovative device-based drug delivery solutions that improve tissue exposure when systemic delivery is insufficient. This hybrid role involves close collaboration with Discovery and Development Biological Sciences to understand delivery barriers, assess breakthrough technologies, and champion strategies that could transform how therapies reach the CNS.

In this highly strategic and scientific role, you'll drive preclinical study design, analyze biodistribution and efficacy data, and co-author impactful publications that influence the scientific community. The ideal candidate will bring a Ph.D. in Biomedical Engineering or M.D. in Neuroscience/Neuro-Oncology, extensive CNS drug delivery experience, and excellent scientific writing skills. If you're looking to shape translational research and make a tangible impact on future clinical development, this could be your next career milestone.

location: North Chicago, Illinois

job type: Contract

salary: $69.00 - 97.50 per hour

work hours: 9 to 5

education: Masters

Responsibilities

  • Supplier Due Diligence: Execute due diligence on potential device suppliers, emphasizing those with capabilities to facilitate pathways to clinical trials and commercial launches. Partner with medical device suppliers throughout early development stages.
  • Preclinical Study Design: Collaborate in developing study protocols by providing expert insights to enhance device performance and achieve targeted endpoints effectively.
  • Data Analysis and Presentation: Analyze and interpret data from preclinical studies, focusing on drug biodistribution, efficacy, and toxicity. Co-author presentations designed to assist stakeholders in making informed project milestone decisions.
  • Publications: Co-author and co-edit white papers and external publications to share insights and findings with the broader scientific community.

Qualifications

Required Skills / Qualifications

  • Ph.D. in Biomedical Engineering or M.D. in Neuroscience/Neuro-Oncology
  • 5 years of pharma and/or biotech relevant industry experience
  • Demonstrable experience with drug delivery to the Central Nervous System (CNS), including:
    • Surgical procedures
    • Use of medical devices
  • Proven ability to independently draft peer-reviewed research papers
  • Strong editing, reviewing, and revising skills for scientific manuscripts
  • Excellent communication and collaboration skills (especially with co-authors and editorial boards)
  • Must be local to Illinois (IL), specifically commutable to North Chicago / Lake County
  • Must be willing to work onsite on a hybrid schedule
  • Must be willing to work between 20-40 hours per week
  • Must be authorized to work in the U.S. with no current or future sponsorship requirements
Preferred / Nice-to-Have Skills

  • Experience in:
    • Supplier due diligence (especially with device suppliers for clinical trials and commercial launch)
    • Preclinical study design (enhancing device performance, achieving targeted endpoints)
    • Data analysis related to biodistribution, efficacy, toxicity
    • Creating stakeholder presentations for milestone decisions
    • Co-authoring white papers and scientific publications
  • Strategic thinking and ability to translate preclinical data into clinical development
  • Ability to shape and champion early-stage drug/device delivery concepts
skills: Editing, Clinical research, Data Analysis, Clinical Data Management, Drug Safety, Medical Device Product Development

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).

This posting is open for thirty (30) days.

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Salary : $69 - $98

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