Laboratory Technician​/Clinical Research Coordinator

Laboratory Technician / Clinical Research Coordinator

• Full-time
• Compensation: up to USD 18 - hourly

Eurofins Scientific is an international life sciences company, providing analytical testing services to clients across multiple industries to help keep life and 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 leading companies to ensure product safety, authentic ingredients, and accurate labeling.

The Eurofins network is a global leader in food, environment, pharmaceutical and cosmetic product testing, and in genomics, discovery pharmacology, forensics, and advanced material sciences. It also supports clinical studies and has a growing presence in Contract Development and Manufacturing Organizations, specialized molecular clinical diagnostics, and in vitro diagnostic products.

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

In 2024, Eurofins generated total revenues of EUR €6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.

The General Laboratory Technician role is an entry-level position in the Clinical Services department at Eurofins CRL, Inc. The Eurofins CRL, Inc. (ECRL) Texas location serves pharmaceutical, cosmetic and personal care product industries by performing safety, efficacy and consumer perception studies in vivo and in vitro, in compliance with applicable Good Laboratory Practices (GLPs) and Good Clinical Practices (GCPs).

The Technician reports directly to the Clinical Services Manager and is involved in a multitude of different testing and lab activities in clinical settings. Testing and techniques include Human Repeat Insult Patch Testing, Clinical Safety-In-Use testing, Bio-instrumental efficacy testing, and more. This position will require heavy administrative work performed electronically (such as generating study documents, data entry on Excel and Word, reviewing study results) and through physical documents as it relates to onboarding, conducting, and concluding Clinical Research Studies within a projected timeline.

• Maintain a safe, fast-paced, and positive laboratory environment.
• Follow all applicable Good Laboratory Practice regulations.
  • Follow all protocol and SOPs, reporting any deviations promptly to Study Director.
  • Note and inform Study Director of any unforeseen circumstances that may affect the quality and integrity of the study.
• Follow all applicable Good Clinical Practice regulations.
  • Obtain informed consent from human test subjects in a GCP setting.
  • Obtain background health information from prospective study subjects to evaluate their eligibility to participate in Eurofins CRL, Inc. clinical trials.
  • Obtain HIPAA Authorization from prospective study subjects.
  • Coordinate with Principal Investigator to ensure adequate subject recruitment has been met for each study.
  • Interact directly with clients on an as-needed basis.
  • Perform delegated duties assigned by Principal Investigator.
  • Responsible for the technical conduct of assigned tasks.
  • Follow all protocol and SOPs, reporting any deviations promptly to Principal Investigator.
• Responsible for the technical conduct of assigned tasks in the Clinical Services department. Tasks include preparation of study materials, study conduct, and executing clinical studies with human subjects.
  • Preparation of study materials requires strong attention to detail and organizational skills.
  • Performing study conduct after adequate training, including patching for sensitization tests, and performing basic dermal evaluations of study subjects.
  • Performing testing methodologies with clinical subjects involves informed consent of volunteers, eligibility screening, and leading subjects through testing methodologies and study requirements.
• Make certain that all experimental data, including observations of unanticipated…