Clinical Project Manager
Eurofins Agroscience Services North Carolina
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 Organization 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 Organizations. It also has a rapidly developing presence in highly specialized 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 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. Lead and/or support regional teams in the execution of projects and to excel in service performance and delivery. To deliver superior performance (time, quality, cost, and service) to exceed the clients’ expectations and specifications and continued business relationship. Project Manager Duties Include but are not Limited to the Following: Oversee project conduct to provide a pro-active and timely project/study communication with theclients to maximize client satisfaction and continuing relationships as the primary point of contactbetween the Clinical team and ECL Ensure accurate, timely and efficient study execution according to clinical protocol/quote within theregional scope of the project Ensure that the project is conducted in accordance with project management global standards andprocedures of ECL Ensure that client’s formal approval on specifications, incl. amendments, are obtained before puttinginto production Ensure all study activities (set-up, conduct, closure) are delivered on-time, in full (on specs) and withinbudgets 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 elevate to/follow-through with Head PM, other functional and siteleaders if services and projects deviate from expectations Ensure that the Study File is accurate, maintained, complete, and self-explanatory such that it will passa regulatory inspection during the life time of the study, and at any time after closure in line with theprevailing 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 fluiddrug development services business environment Senior Project Managers will support Global Project Managers on global studies in their region Perform other duties assigned my manager Basic Minimum Education Qualifications: Project Manager: A Bachelor degree in healthcare/life sciences (laboratory or clinical services preferred) or significant industryexperience (5+ years) in Central Lab is also considered acceptable. Basic Minimum Work Requirements: Project Manager: Minimum of 2 - 4 years Project Management experience in complex project service industries Minimum of 2 - 4years relevant clinical project experience with a CRO or Sponsor organization Authorization to work in the United States indefinitely without restriction or sponsorship. The Ideal Candidate Possesses the Following: Energetic and enthusiastic person, willing to travel as required to attend investigator meetings, othernecessary client meetings, and internal global meetings. Fuent in English, other languages of operating sites and global clients of advantage A proven track record of strong customer focus, driven by quality and exceptional level of service Possess excellent communication skills, with the ability to assimilate and rationalize large volumes ofinformation and determine best course of action. Excellent communication skills being to assimilate large volumes of information and requests todetermine the best course of action Good organizational and analytical skills, client service focus and performance orientation Position is full-time working remotelyMonday - Friday, 8:00am - 5:00pm, andadditional hours as needed. 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 Clinical Trial Solutions is a Disabled and Veteran Equal Employment Opportunity employer. #J-18808-Ljbffr Eurofins
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...Clinical Project Manager - Oncology (Client Dedicated/Remote) Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes...Contract workWork at officeRemote workWorldwideFlexible hours- ...Job Description Summary We’re looking for a Clinical Research Coordinator to support cutting-edge research that helps shape the future... ...scheduling participants, reserving space, ensuring staff training, and managing documentation Ensure compliance with the study protocol,...Work at officeVisa sponsorshipWork visaRelocation package
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...across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of... ...drivers. The CRCs assist with the maintenance of participant management and data management on research/clinical studies.Role Overview...Full timeMonday to FridayFlexible hoursShift workAfternoon shift$25 - $35 per hour
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Join to apply for the Clinical Research Coordinator - PACC role at Columbia University Irving Medical Center Join to apply... ...of research subjects for our ongoing clinical research projects. Responsibilities Manage study participants by facilitating screening, enrollment...Full timeTemporary workWork at officeLocal area$70.48k - $74.79k
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