Experienced scientist with a demonstrated history of working in the clinical research and medical device industries. Strong research professional skills in data analysis, laboratory practices, biology, project management, and training. I empower team cohesiveness to better meet project deadlines, improve processes, and ultimately achieve company goals.

My goal is to utilize my background in medical device development, validation, transfer, and manufacturing as well as my  recently attained education in clinical trial management to explore and achieve in clinical trial monitoring work. 

Areas of Expertise
  • Quality Assurance
  • Medical Device Development and Regulation 
  • Data Analysis 
  • Clinical Trial Management 
  • Good Documentation Practices (GDP)
  • Good Clinical Practice (GCP)
  • Good Laboratory Practice (GLP)
  • Good Manufacturing Practice (GMP)
  • Regulatory Affairs & Compliance
  • Leadership & Team Building
  • Internal / External Audits
  • Standard Operating Procedures (SOPs)


Amanda Albers, MS

Production Supervisor, MiraVista Diagnostics

Indianapolis, IN


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