Clinical Research Coordinator

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.

Pay Range: $20.00/Hr.

Shift: Monday- Friday, 9:30am- 6:00pm

Primary Duties and Responsibilities of a CRC

• Act as project manager on studies as directed by department manager.
• Assist in the conduct of clinical studies as specified by the study protocol under the supervision of designated Principal Investigator and departmental management.
• Record observations, measurements, and test results, as required.
• Provide a professional experience to test subjects, and answer all inquiries, as appropriate
• Assist in the preparation of test materials, as needed.
• Perform data entry and data review to ensure study quality.
• Conduct studies in accordance to ECRL Standard Operating Procedures study protocol and ICH GCP.
• Efficiently time manage multiple projects.
• Succinctly communicate day to day project details to both department manager and Principal Investigator.
• Perform department specific procedures as qualified by training and evaluation of proficiency (clinical study evaluations and measurements)
• Process study data and prepare for reporting and conclusions.
  
  

• High School Diploma
  
  

What we offer:

• Excellent full time benefits including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays

Eurofins USA Consumer Product Testing is a Disabled and Veteran Equal Employment Opportunity employer.