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Consultant Pediatrician
2 months ago
Job Description
We assure you, this will be the easiest job you have ever had Consulting pediatricians will visit Eurofins CRL in Austin Texas, directly prior to and following the use of the assigned test product for each study. Most studies require 35-50 subjects, which we typically process in 3-4 hours. ECRL staff will perform all logistical management of study subjects, including consenting, handing out products, and datasheet/paperwork completion. Consulting pediatricians will observe the body part where the product is being used (e.g. arms and legs, face, torso, diaper region, etc.) for signs of irritation.
Depending upon the needs of our clients, some studies may not require a pediatrician to perform examinations, only review study results. In such cases the consulting pediatrician will be listed as the Principal Investigator or Sub-Investigator and be required to review and sign a written protocol prior to study initiation. In instances where the pediatrician is not required to perform evaluations, trained ECRL staff will perform the evaluations per the protocol, and the pediatrician will then review and sign the Final Report once the study is complete.
When a study is commissioned, we would contact you to determine your availability, then schedule approximately 4-8 hours for the baseline visit and 4-8 hours for the follow up visit (typically occuring 2-4 weeks after baseline) at your convenience. Currently our needs may be sporadic, but eventually we hope to increase business so that we may need you for 2 or more studies a month. The option to decline participation would be available for all studies.
Qualifications:
Qualifications
Required Qualifications:
Valid, unrestricted medical license for U.S. practice.
Ability to treat at clinical study subjects with respect and courtesy.
Ability to provide timely and accurate assessments of your personal schedule to Vivo Clinical Testing.
Ability to receive and review electronic documents (PDF, .docx, etc.) in a timely manner based on communicated scheduling.
Authorization to work in the United States indefinitely without restriction or sponsorship
Desired Qualifications:
Certification through the American Board of Pediatrics ("board-certified").
Flexible availability for on-site work at Vivo Clinical Testing.
Prior experience working in a commercial or clinical testing lab.
Knowledge of, and experience with FDA Good Clinical Practice (GCP) regulations.
Understanding of statistical analysis (ANOVA, T-test, etc.) sufficient to allow understanding of report data.
Major Duties:
Perform dermal evaluations of children participating in clinical studies.
Review and approve clinical study protocols.
Review and approve clinical study data within the context of Final Reports.
Interact with and provide detailed and accurate scheduling information to laboratory personnel.
Participate in a safe, fast-paced, and positive laboratory environment.
Additional Information
- COMPREHENSIVE BENEFITS PACKAGE & COMPENSATION
As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options.
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
\ #LI-EB1
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
