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
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## Clinical Research Coordinator IApplylocations: 3316 Rochambeau Avenuetime type: Full timeposted... ...studies, and quality improvement projects within the department of Neurology,... ...Coordinator I is expected to be able to manage clinical trial projects independently after...Shift work- ...Clinical Research Coordinator (CRC) IIA Clinical Research Coordinator (CRC) II position is currently available within the Tisch Cancer... .... Duties will include activities such as data collection and management of patient clinical information, timely collection of protocol...TraineeshipWork at officeLocal areaShift work
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...States of America) Salary Range: $54,690.00 - $82,035.00 Clinical Research Coordinator Hemophilia Program Albany, NY The... ...of research; coordinates contractual issues related to research projects; establishes and maintains communications throughout the study...Full timeLocal areaShift work- ...DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator II... ...by Sponsor approved protocol Study IP management Provide training and guidance for new... ...best practices for data entry portals and project workflows Interact with Principal Investigator...Full time
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Fortrea is seeking Clinical Trial Managers to join our team! We are seeking experienced CTLs with 3+ years of experience. Remote US or Canadian... ...of clinical research trials. This role collaborates with project managers and other functional leads to deliver clinical and...Contract workWork at officeRemote work- ...enrollment, grant submissions, and data collection in accordance with Good Clinical Practices, HIPAA, and sponsor requirements. You will liaise with Research Nurses, Pharmacists, Program Managers, and IT/regulatory staff, monitor study progress, assist with budget #J-1...
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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
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