Job Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

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

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.

Job Tags

Holiday work, Full time, Contract work, Flexible hours,

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