Study Director - Biocompatibility Studies

Added
8 days ago
Type
Full time
Salary
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iso standards epa fda dot regulatory compliance
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πŸ“‹ Description

  • Supervise and assist in the conduct of regulatory studies performed
  • Supervise study conduct
  • Assist in protocol development, design and implementation
  • Responsibilities as stated in GLP regulations
  • Data interpretation and report writing
  • Client liaison

🎯 Requirements

  • BS degree in a field related to their area of responsibility (e.g. animal science, chemistry
  • Minimum of 5 years experience overseeing biocompatibility studies
  • Intimate working familiarity and/or ability to quickly learn and develop such familiarity with all
  • Hands-on working knowledge of the tests that will be under their responsibility
  • Good administrative skills and leadership ability
  • Must communicate effectively and write well

🎁 Benefits

  • Position is full-time, Monday-Friday, 9:00am-5:00pm, with overtime as needed
  • Equal Opportunity Employer
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