Consultant Gynecologist
Consultant Gynecologist
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Job Description
We assure you this will be the easiest job you have ever had! Consulting gynecologists will visit Eurofins CRL in Austin Texas directly prior to and following the use of assigned test products for each study by participating subjects. Most studies require 3550 subjects but can vary depending on study design which we typically process in 36 hours. ECRL staff will perform all logistical management of study subjects including consenting handing out products and datasheet/paperwork completion. Consulting gynecologists will observe the body part where the product is being used for signs of irritation as well as perform other gynecological evaluations as specified by the sponsor approved study protocol.
When a study is commissioned we would contact you to determine your availability then schedule approximately 48 hours for the baseline visit and 48 hours for the follow up visit (typically occurring 24 weeks after baseline) at your convenience. We are currently seeing an uptick of Gynecologist Safety In Use studies so we are looking for a gynecologist with availability on Thursdays. The option to decline participation would be available for all studies.
Qualifications :
Required Qualifications:
Valid unrestricted medical license for U.S. practice.
Ability to treat clinical study subjects with respect and courtesy.
Ability to provide timely and accurate assessments of your personal schedule to Eurofins CRL within 2448 hours.
Ability to receive and review electronic documents (PDF .docx etc.) in a timely manner based on communicated scheduling.
Desired Qualifications:
Be a BoardCertified Gynecologist
Flexible availability for onsite work at Eurofins CRL preferably on Thursdays.
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 Ttest etc.) sufficient to allow understanding of report data.
Major Duties:
Perform gynecological evaluations on female subjects ranging from 1875 years of age.
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 fastpaced and positive laboratory environment.
Additional Information :
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 fulltime 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.
Authorization to work in the United States without Sponsorship
Eurofins is a M/F Disabled and Veteran Equal Employment Opportunity and Affirmative Action employer.
Eurofins USA Consumer Product Testing is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Fulltime
Employment Type
Full-time
