Sr. Field Clinical Research Specialist
Medtronic, Inc. · Minneapolis, MN telecommuting permitted
Experience must include
GCP and regulatory compliance guidelines for clinical trialsClinical Trial Design and Execution (Phase I-IV)Clinical study Start-up, site initiation, monitoring, and close-outICF and Protocol development and reviewPatient recruitment and retention strategiesSource document verification (SDV)Adverse event (AE) and Serious adverse event (SAE) reportingFDA Regulations 21 CFR Parts 11, 50, 54, 56, 312, 812ICH-GCP (E6 R2/R3) ComplianceIRB/IEC Submission and approval processCAPA development and implementationHIPAA compliance
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Application instructions (verbatim)
Apply at. https://jobs.medtronic.com/ Req. #R77878 Medtronic is an equal opportunity employer. All individuals are encouraged to apply.
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Why we think this is a PERM ad (92% confidence): This posting exhibits multiple hallmarks of a PERM labor-test advertisement: it names the specific employer (Medtronic, Inc.) and worksite (Minneapolis, MN / greater Chicago metro area remote); states exact minimum requirements including 'Master's degree in Biological Science, Biology, Nursing, Biomedical Engineering, or Biotechnology and two (2) years of experience as a Clinical Researcher or related occupation' with detailed specific experience requirements ('at least two (2) years' experience with each of the following: GCP and regulatory compliance...'); provides a specific requisition ID (R77878) for application; and includes the phrase 'or related occupation' which is standard PERM language. The posting is form-like and terse despite the extensive job duties, with emphasis on exact qualifications rather than company culture.