Fresenius Medical Care Job - 33129303 | CareerArc
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Company: Fresenius Medical Care
Location: New York, NY
Career Level: Entry Level
Industries: Healthcare, Pharmaceutical, Biotech


Job ID 20000DK4

Available Openings 1

Position Specific Information

Research Scientist, Renal Research Institute, LLC, a Fresenius Medical Care N.A. company, New York, NY

Purpose and Scope:

Responsible for assisting with the planning, design, and execution of research studies and producing high-quality and accurate research reports and publications in the fields of renal and kidney disease/failure and nutrition.

Principal Duties and Responsibilities:
  • Planning, collaborating, and conducting research and development activities for all phases of human subject research.
  • Collecting, storing, and maintaining research data.
  • Preparing abstracts, conference posters/talks, and manuscripts for publication in peer-reviewed scientific journals as required.
  • Organizing technical reports, summaries, presentations and quantitative analyses for presentation to appropriate personnel, externally and internally.
  • Preparing and submitting regulatory documents to appropriate board or agency, including the Institutional Review Board (IRB).
  • Designing protocols and human research subject Informed Consent procedure development.
  • Investigating, creating and developing new methods and technologies for project advancement.
  • Preparing sample analysis and/or sample preparation for analysis /shipping.
  • Assists with data analysis and explores techniques involved in biostatistical analytics.
  • Presenting research findings at scientific conferences and meetings.
  • Other duties as assigned.

Education Experience and Required Skills:

Position requires a Master's degree (or equivalent foreign degree) in Biology, Chemistry, Nutrition, Physiology, Biomedical or Health Sciences or a closely related life sciences field and 1 year of experience as a Research Assistant. Experience (which may be gained concurrently with the primary experience requirement above) must include:

  • Planning and conducting research and development activities for human subject research, including screening, consenting and enrolling study subjects; conducting study visits; conducting training to study sites; assisting in study monitoring and auditing; and organizing study data and analysis.

  • Working knowledge of basis biostatistical techniques: distribution analysis, t-test, ANOVA and linear regression; analyzing and visualizing study data using statistical software python and SAS.

  • Presenting research findings to an audience of scientists or healthcare professionals.

  • Training in Good Clinical Practice (GCP) International Council for Harmonisation (ICH) E6 guideline and FDA guidelines Title 21 of the Code of Federal Regulations (21 CFR).

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