Clinical Research Assistant

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 is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins 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. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. 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.

This role reports to the Clinical Manager and is part of a new team with the Eurofins network, supporting Phase I-III IND clinical trials with Hair, Skin and Nail evaluation endpoints. We will train the right candidate but experience in any discipline of Clinical research (especially from a regulatory aspect) is a plus. You will work closely with a small team inclusive of 2 Principal Investigators in Dermatology.

Responsibilities

Project support inclusive of project planning, Preparation of paperwork and documentation, and maintaining study participant records.; Data collection; Audits (both virtual and in person); General preparation and closing of studies; Working with IRB submissions; Assisting with Study participant recruitment inclusive of phone and in person screening and subject scheduling; Executing Study participant visits inclusive of subject vitals (possibly Phlebotomy but will train) , electronic data entry, visual evaluations and PI assistance.; Clinical Trial data entry; Other tasks as dictated by business needs and the Clinical Manager

Requirements

Certified CRA credential ideal; Minimum 1+ years expereince in clinical research; Experience in regulatory aspects of Phase I-III clinical IND trials and experience with FDA audits.; Experience with Microsoft platforms, EMR and EHR (electronic health record) systems and CTMS strongly preferred.; Experience with phlebotomy preferred.; Authorization to work in the United States indefinitely without restriction or sponsorship.

Benefits

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