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 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. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized 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 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. Job Description 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. Clinical Research Assistant responsibilities include, but are not limited to, the following 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. Basic Minimum Qualifications Certified CRA credential ideal Minimum 1+ years experience 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. Position Full-time working Monday - Friday 9:00 am - 5:00pm. Candidates must be within a commutable distance to Forest, VA. 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 Eurofins USA Consumer Product Testing is a Disabled and Veteran Equal Employment Opportunity employer. #J-18808-Ljbffr Eurofins Consumer Product Testing