Lavori attuali relativi a Clinical Trial Manager - Milano - Precision For Medicine
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Clinical Trial Manager
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Clinical Trial Manager
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Clinical Trial Manager
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Clinical Trial Manager
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Clinical Trial Manager
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Clinical Trial Operations Manager
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Clinical Trial Operations Manager
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Junior Clinical Trial Manager
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Clinical Trial Manager
1 settimana fa
Milano, Lombardia, Italia Bancroft School A tempo pienoUnlock Your Potential as a Clinical Trial ManagerMedpace, a leading Contract Research Organization (CRO), is seeking an experienced Clinical Trial Manager to join our team in Italy, specifically in our Milan office. As a Clinical Trial Manager, you will play a crucial role in managing and providing accountability for day-to-day operations of clinical trials,...
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Clinical Trial Manager
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Clinical Trial Manager
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Milano, Lombardia, Italia Medpace, Inc. A tempo pienoJob SummaryMedpace, Inc. is seeking a highly skilled and motivated Clinical Trial Manager to join our Clinical Trial Management team. The successful candidate will be responsible for managing clinical trials from start to finish, ensuring timely delivery of tasks and maintaining high accuracy standards.Key ResponsibilitiesCommunicate and collaborate with...
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Clinical Trial Manager
3 settimane fa
Milano, Lombardia, Italia Medpace, Inc. A tempo pienoJob SummaryMedpace, Inc. is seeking a highly skilled and motivated Clinical Trial Manager to join our Clinical Trial Management team. The successful candidate will be responsible for managing clinical trials from start to finish, ensuring timely delivery of tasks and maintaining high accuracy standards.Key ResponsibilitiesCommunicate and collaborate with...
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Clinical Trial Ambassador
5 mesi fa
Milano, Italia Syneos Health Clinical A tempo pieno**Overview** The Clinical Trial Ambassador will establish, cultivate, and maintain scientific relationships with investigators and study coordinators to support enrollment while developing a strong understanding of clinical practice as it relates to areas of interest. This position interacts with various internal and external stakeholders, with a focus on...
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Clinical Trial Manager
6 giorni fa
Milano, Lombardia, Italia Bancroft School A tempo pienoUnlock Your Potential as a Clinical Trial ManagerMedpace, a leading CRO, is seeking an experienced Clinical Trial Manager to join our team in Italy, particularly in our Milan office. As a key member of our Clinical Trial Management Group, you will be responsible for managing and providing accountability for day-to-day operations of projects, ensuring...
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Clinical Trial Manager
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Clinical Trial Manager
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Clinical Trial Coordinator
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Milano, Lombardia, Italia ICON A tempo pieno{"title": "Clinical Trial Assistant", "description": "Job SummaryICON plc is a world-leading healthcare intelligence and clinical research organization. We advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device, and government and public health organizations.As a Clinical Trial Assistant, you will support...
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Sso Clinical Trial Associate
4 mesi fa
Milano, Italia Novartis A tempo pieno100,000+ That’s how many patients participate in our clinical trials at any given time. GCO (Global Clinical Operations) is Novartis’ powerhouse of Global Clinical Operations, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access for patients to potential novel treatments. Every day, we are the link...
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Clinical Trial Manager
4 mesi fa
Milano, Italia Icon plc A tempo pienoICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. - With our patients at the centre of all that we do, we help to accelerate the...
Clinical Trial Manager
4 mesi fa
We have current opportunity for an experienced Clinical Trial Manager in Europe Join our growing team.
Precision for Medicine is a precision medicine CRO. Precision's uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas.
You will be the hub of central intelligence for the studies you will be managing, and will lead CRAs and oversee all clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. We encourage high-energy, dedicated professionals who enjoy a challenge, thrive in the details and flourish in dynamic environments to explore this opportunity.
We are addressing the challenges facing the research and development of novel compounds in Oncology and are dedicated to positively impacting the health and lives of patients around the world. If you take a consultative approach to trial management, proving to be a valuable partner in the trial operational delivery process, don't miss exploring working with us.
We offer flexible location options, and remote based working. This position can be based in one of the following countries: Spain, UK, Poland, Hungary, Serbia. Romania, Slovakia.
About You: You love having responsibility and a say in how clinical trials are run You plan ahead, but have alternative options and a flexible approach You are client focused and You are well organised and able to manage timelines and shifting priorities, without sacrificing quality. You communicate clearly, often and concisely and know that your role is crucial in keeping the trial running smoothly You are a master at identifying any risks that threaten projects and handle them resolutely You thrive and work with autonomy and ownership to deliver successful outcomes The day-to-day role, and how we will support your continued growth: Management and operational delivery of the clinical elements within a trial including site selection, start-up, enrollment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out Successful execution of assigned trials and ensuring completion of trial deliverables Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by working in close collaboration with other functional team members Mentoring and training of team members Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve the highest level of client satisfaction Qualifications: Bachelor's degree or equivalent combination of education/experience in science or health-related field, including experience in the field of oncology Other Required:
Demonstrable experience leading clinical aspects of your studies across multiple countries in a CRO / Pharma or Biotech company (in a dedicated 'clinical lead' role). Working knowledge of GCP/ICH guidelines and the clinical development process Availability for domestic and international travel including overnight stays Skills:
Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS) Demonstrated ability to develop positive working relationships with internal and external organizations Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan Demonstrates mastery knowledge of ICH-GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.
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