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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 50,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialized clinical diagnostics testing.

In 2020, Eurofins generated total revenues of EUR‚ 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.

·       Assist in the preparation of study protocols, amendments, deviations, data capture forms, test article documentation and study reports

·       Collaborate with multiple internal partner groups to plan, coordinate, conduct, analyze, and report studies

·       Conduct training of Investigators and other study site personnel

·       Serve as the principal communication link between the Sponsor and study sites

·       Maintain study files in accordance with SOPs and regulatory requirements

·       Assist in data management processes including paper and electronic data capture, entry, review, tracking and verification utilizing electronic tools and centralized data management systems.

·       Assist in preparation of study files for submission to regulatory agencies

·       Provide clinical updates to project teams and sub-teams

·       Assist with animal related study activities (i.e. clinical sampling, test material administration and clinical observations)

Position is full-time, Monday-Friday 8:00 a.m.-5:00p.m., with overtime as needed. Candidates currently living in a commutable distance to Kalamazoo, MI are encouraged to apply.

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 is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.