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 47,000 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 specialised clinical diagnostics testing.
In 2019, Eurofins generated total revenues of EUR 4.56 billion, and has been among the best performing stocks in Europe over the past 20 years.
Serves as key support to the PI team to execute important and timely administrative duties to keep projects on time, within budget, and within regulatory compliance.
Liaise with other departments (Lab Ops, Sample Management, Scientific Affairs, QA, Report Writing, Business Development, etc) as necessary to execute on the project plan, developing and maintaining timelines
Responsible for interface with Business Development to ensure change orders are timely if needed.
Creates draft sample analysis outlines to review with PI and manages amendments..
Creates study blueprint for ,kickoff provides meeting agenda
Schedules client meetings, provides and maintains meeting minutes and agendas as needed
Maintains necessary Smartsheet updates as required by other departments
May assist PI with worklisting for Sample Analysis
Develops and maintains good working relationships with Sponsors, interfacing with Business Development, and Scientists to communicate and meet Sponsor needs and timelines
Works with Sample Management, PIs, Sponsors, and 3rd party central labs/clinical sites to resolve manifest, sample labeling, sample reconciliation issues
Works with PI to organize resource allocation/scheduling, contributes to company forecasts and revenue recognition based on project specifications and timelines.
Designs and improves processes and procedures to increase efficiency, productivity, and quality
Arranges specimen and data handling for all services
Oversees study records, data and sample storage
Organizes all documents for interim archive submission
Conducts closeout process including archiving, sample disposition document management for technical writers
Coordinates transfers of hard copy project records to Quality for archiving
Maintains accurate client databases
Assists with the writing of company SOPs and facilitates the upload of documents into EtQ by providing to QAU.
Applies GxP in all areas of responsibility, as appropriate
Works effectively as a member of a team, under minimum direction to achieve client and business deadlines.
Attends internal and external training courses.
Demonstrates and promotes the company vision
Regular attendance and punctuality
Conducts all activities in a safe and efficient manner
djusts work hours as needed to meet client deadlines
Adheres to site employee health and safety (EHS) requirements
Performs other duties as assigned
The Ideal Candidate would possess:
Basic Minimum Qualifications:
Bachelor's Degree (preferably a B.S.) in a science, accounting, or related field requiring analytical thinking skills
1-5 years' experience in drug development
Authorization to work in the United States indefinitely without restriction or sponsorship
Position is full-time, Monday
5:00pm. Candidates currently living within a commutable distance of St Charles, MO are encouraged to apply.
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.