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.
This is a full-time position, Monday-Friday 8:00am-5:00pm, based in Boston, MA.
What we offer:
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
Conduct onsite monitoring across clinical studies, oversee site communication and study progress, review clinical data, resolve queries, and support study startup and regulatory submissions.
Conduct clinical trial site monitoring from selection through closeout, support investigators and study teams with training and communication, and help maintain study quality, documentation, and progress.
Apply clinical and scientific expertise to human health consulting matters, researching and evaluating evidence and helping prepare reports for legal, insurance, and other clients.
Conduct onsite monitoring across Phase II and III clinical studies, manage site communications and study documentation, and coordinate with project teams, vendors, and support services.
Create and evaluate clinical nutrition cases, chart-review scenarios, reference answers, and rubrics, applying dietetic expertise to assess AI outputs for accuracy, safety, and sound clinical reasoning.
