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 product’s for each study by participating subjects. Most studies require 35-50 subjects but can vary depending on study design, which we typically process in 3-6 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 4-8 hours for the baseline visit and 4-8 hours for the follow up visit (typically occurring 2-4 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 24-48 hours.

Ability to receive and review electronic documents (PDF, .docx, etc.) in a timely manner based on communicated scheduling.

Desired Qualifications:
Be a Board-Certified Gynecologist

Flexible availability for on-site 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, T-test, etc.) sufficient to allow understanding of report data.
Major Duties:
Perform gynecological evaluations on female subjects ranging from 18-75 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, fast-paced, 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 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.

• 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.