Remote Field Applications Lead for IsoPSA Lab Implementations

Cleveland Diagnostics

Cleveland (OH)

Remote

USD 80,000 - 100,000

Full time

14 days+
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Benefits offered by this job

100% Employer-paid medical for single
4% retirement contribution Employer m
Stock Option Program
Flexible work schedule

Job summary

Cleveland Diagnostics is seeking a Field Applications Specialist to lead the IsoPSA implementation in customer labs. The role requires extensive travel (up to 80%) to on-site customer sites and collaboration with the CDx team to ensure successful deployment.

You will plan workflows, train customers, validate assays, and provide post-implementation support, while maintaining strict adherence to GLP, HIPAA, and regulatory requirements. On-site travel is essential to success.

Qualifications

  • BA/BS in Chemical, biological or clinical laboratory science.
  • MT (ASCP) or MLS (ASCP) certification preferred.
  • Five years of experience working in clinical or CLIA lab environment.
  • Must have the technical expertise and experience to implement IsoPSA in a Clinical Laboratory.
  • Must possess a positive customer attitude.
  • Must be able to travel extensively, up to 80%.
  • Excellent computer skills: Word, Excel, PowerPoint, Salesforce.com.

Responsibilities

  • Design plan to implement IsoPSA at CDx customer labs.
  • Execute IsoPSA IVD implementations at CDx customer labs.
  • Provide ongoing technical support to CDx IVD customers post-implementation.
  • Other duties as assigned.

Skills

Lab experience
Travel 80%
Customer focus
Troubleshooting
Interpersonal communication

Education

BA/BS in Chemical, biological or clinical laboratory science

Tools

Salesforce.com
LIS systems
EMR systems

Job description

Cleveland Diagnostics is seeking a Field Applications Specialist to lead the IsoPSA implementation in customer labs. The role requires extensive travel (up to 80%) to on-site customer sites and collaboration with the CDx team to ensure successful deployment.

You will plan workflows, train customers, validate assays, and provide post-implementation support, while maintaining strict adherence to GLP, HIPAA, and regulatory requirements. On-site travel is essential to success.

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