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.
Oversee project conduct to provide a pro-active and timely project/study communication with the clients to maximize client satisfaction and continuing relationships as the primary point of contact between the Clinical team and Eurofins GCL
Ensure accurate, timely and efficient study execution according to clinical protocol/quote
Ensure that the project is conducted in accordance with project management global standards and procedures of Eurofins GCL
Ensure that client's formal approval on specifications, incl. amendments, are obtained before putting into production
Ensure all study activities (set-up, conduct, closure) are delivered on-time, in full (on specs) and within budgets and oversee corrective actions to bring them back on track and expectations
Maintain complete financial management of the budget for assigned studies
Take appropriate actions and escalate to/follow-through with PM Team Leaders, other functional and site leaders if services and projects deviate from expectations
Ensure that the Study File is accurate, maintained, complete, and self-explanatory such that it will pass a regulatory inspection during the life time of the study, and at any time after closure in line with the prevailing regulations at the time of the study
When required, actively support sales in bid process to gain repeat, and/or new, long-term business
Support and work with QA, be present during the study audit, and present the study file
Ensure timely resolution of corrective actions assigned to the Project Manager
Execute projects within timelines and on budget
Lead, manage, and support assigned projects to surpass global standards in a competitive and fluid drug development services business environment
The ideal candidate would possess :
Driven by quality and service levels
Energetic and enthusiastic person, willing to travel as required to attend investigator meetings, other necessary client meetings, and internal global meetings
Excellent communication skills being to assimilate large volumes of information and requests to determine the best course of action
Good organizational and analytical skills, client service focus and performance orientation
Fluent in English, other languages of operating sites and global clients of advantage
Reports to Team Leader PM
Primary point of contact with client's clinical team
Wider client community
Collaborates with team leaders, project management staff, data management staff, and global functional groups
Collaborates with sales
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Basic Minimum Qualifications :
Bachelor's degree in biology, chemistry, or other related degree concentration.
Two years relevant experience in the life science, pharmaceutical or laboratory services industry; hands-on clinical trials experience preferred
Authorization to work in the United States indefinitely without restriction or sponsorship
Position is full-time, Monday - Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of Lancaster, PAare 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.
Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.