Lavori attuali relativi a Clinical Trials Vendor Management Specialist - Milano - Psi Cro
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Clinical Trials Site Identification Specialist
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Milano, Lombardia, Italia Psi CRO Ag A tempo pieno{"h3": "Clinical Trials Site Identification Specialist Job Description"} At PSI CRO Ag, we're seeking a skilled Clinical Trials Site Identification Specialist to join our team. As a key member of our clinical trials team, you'll play a crucial role in identifying and evaluating potential clinical trial sites, ensuring the success of our studies. Key...
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Clinical Trials Site Identification Specialist
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Milano, Lombardia, Italia Psi CRO Ag A tempo pienoJob DescriptionRole SummaryWe are seeking a highly skilled Clinical Trials Site Identification Specialist to join our team at Psi CRO Ag. As a key member of our clinical trials team, you will be responsible for identifying and evaluating potential clinical trial sites, building relationships with medical professionals, and ensuring seamless site start-up...
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Clinical Trials Site Identification Specialist
2 settimane fa
Milano, Lombardia, Italia Psi CRO Ag A tempo pienoJob OverviewPsi CRO Ag is seeking a highly skilled Clinical Trials Site Identification Specialist to join our team. As a key member of our clinical trials operations, you will be responsible for identifying and evaluating potential clinical trial sites, ensuring seamless site initiation and management throughout the study lifecycle.Key ResponsibilitiesSite...
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Clinical Trials Site Identification Specialist
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Milano, Lombardia, Italia Psi CRO Ag A tempo pienoJob OverviewPsi CRO Ag is seeking a highly skilled Clinical Trials Site Identification Specialist to join our team. As a key member of our clinical trials operations, you will be responsible for identifying and evaluating potential clinical trial sites, ensuring seamless site initiation and management throughout the study lifecycle.Key ResponsibilitiesSite...
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Clinical Trials Site Identification Specialist
3 giorni fa
Milano, Lombardia, Italia Psi Cro Ag A tempo pienoJob DescriptionAt PSI, we are seeking a highly skilled Clinical Trials Site Identification Specialist to join our team. As a key member of our clinical trials team, you will be responsible for identifying and evaluating potential clinical trial sites, ensuring the highest quality and compliance with regulatory requirements.Key Responsibilities:Conduct...
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Clinical Trials Site Identification Specialist
7 giorni fa
Milano, Lombardia, Italia PSI CRO A tempo pieno{"h3": "Clinical Trials Site Identification Specialist Job Description"} At PSI CRO, we are seeking a highly skilled Clinical Trials Site Identification Specialist to join our team. As a key member of our clinical trials team, you will be responsible for identifying and evaluating potential clinical trial sites, ensuring that our clients receive high-quality...
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Senior Clinical Research Associate
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Clinical Trials Site Identification Specialist
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Milano, Lombardia, Italia PSI CRO A tempo pienoJob DescriptionJob Summary:We are seeking a highly skilled Clinical Trials Site Identification Specialist to join our team at PSI CRO. As a key member of our team, you will be responsible for identifying and evaluating potential clinical trial sites, developing strategies to accelerate site identification, and providing training to CTAs and CRAs.Key...
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Site Identification and Clinical Trials Coordinator
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Clinical Trials Site Identification Specialist
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Milano, Lombardia, Italia PSI CRO A tempo pienoJob DescriptionOverviewPSI CRO is a leading Contract Research Organization with a strong focus on delivering high-quality services across various therapeutic indications. We are seeking a highly skilled Clinical Trials Site Identification Specialist to join our team.Key ResponsibilitiesStart-up Responsibilities:Collaborate with internal teams and external...
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Milano, Lombardia, Italia PSI CRO A tempo pienoJob DescriptionWe are seeking a highly skilled and experienced Clinical Trials Site Identification Specialist to join our team at PSI CRO. As a key member of our team, you will be responsible for identifying and evaluating potential clinical trial sites, ensuring that our clients' studies are conducted efficiently and effectively.Key Responsibilities:Site...
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Snr Clinical Research Associate
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Vendor Management Specialist
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Statistical Data Analyst
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Clinical Trial Manager
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Clinical Trials Lead Programmer
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Clinical Trials Lead Programmer
2 settimane fa
Milano, Lombardia, Italia Thermo Fisher Scientific A tempo pienoAbout the RoleWe are seeking a highly experienced and motivated Clinical Trials Lead Programmer to join our dynamic team at Thermo Fisher Scientific.Key ResponsibilitiesOversee the statistical and programming aspects of multiple projects, acting as the lead programmer, project lead, or project oversight lead for a client/asset.Play a crucial role in the...
Clinical Trials Vendor Management Specialist
4 mesi fa
We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together almost 3000 dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
Job Description You will be responsible for supporting the establishment of approaches, processes and information flow, along with building strong relationships to ensure effective collaboration between PSI teams and PSI vendors.
You will Review external vendor quotations Maintain vendor databases and tracking systems Support vendor identification, assessment activities, vendor selection and approval processes At a service level, you will assist vendor contracting processes Educate vendors about PSI and maintain vendor relationships to provide high quality, cost-effective external services Review project-specific Vendor Management plans and support study teams with vendor related queries and issues Assist in the development and implementation of quality systems and documents Develop vendor specific KPIs and monitor ongoing performance Conduct training relevant to the vendor management department Qualifications Around 1-3 years of clinical trials experience. Preferably at least 1-year of industry experience in vendor management, proposal development, clinical trial operations, or business development working alongside or managing vendors Good proficiency in MS Office applications C1 level in English language An interest and experience working with project/customer related systems Additional Information Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success. Our recruitment process is easy and straightforward, and we'll be there with you every step of the way. We will guide and support you with information, making your experience as smooth as possible.
We can consider both remote and office based applications.
