504 Posti di lavoro per Site Management in Italia
Mam Site Lead
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Description
Kenvue, part of the Johnson & Johnson Family of Companies (Kenvue),
is currently recruiting for:
MAM Site Lead
**In partnership with the Site Leader and Site Leadership Team, this position serves as the primary point of contact for MS&T including end-to-end MAKE Asset Management from up-front engineering through project delivery as well as ongoing Maintenance and Operations support of MAKE assets at the Pomezia production site.**
This position is based at Pomezia - Santa Palomba (Rome), Italy.
**Who we are**
At Kenvue, part of the Johnson & Johnson Family of Companies, we believe there is extraordinary power in everyday care. Built on over a century of heritage and propelled forward by science, our iconic brands—including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® —are category leaders trusted by millions of consumers who use our products to improve their daily lives. Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers’ hearts and homes.
**What will you do**
The MAM Site Lead is responsible for providing strategic and technical leadership and tactical direction to the diverse and highly skilled team of Engineers, Maintenance Leads, Maintenance Technicians and Capital Project Managers focused on driving and delivering optimal cost, safety, quality and compliance for the Pomezia site manufacturing assets. Reports directly to the Manufacturing, Sciences & Technology (MS&T) Cluster Leader for Skin Health & Essential Health.
Key Responsibilities
- Provides strategic direction and planning for the engineering and maintenance functions at the site aligned with the MS&T Skin Health & Essential Health Cluster and Global Centers of Excellence as well as the Consumer Health Manufacturing EMEA network. Identifies and leads initiatives to drive execution excellence and timely realization of site and network goals and objectives. MAKE Asset Management is structured around 4 functions: Reactive Maintenance (line support), Preventive maintenance (planned), Pro-active maintenance (Reliability) and Design/ Project execution/ Commissioning & Qualification (Engineering)
- Combined responsibility for assets and resources involved with Automation & Controls Engineering including IT/OT systems, Capital Project & Portfolio Management and Production Maintenance including Maintenance Planning, Work Administration & Execution and Strategic Parts Management (MRO)
- Direct, guide and provide oversight for the site CapEx portfolio including forecasting, prioritizing budgeting, controlling and reporting of the site capital plan, communicating status and health to site and network stakeholders.
- Serves as the administrator of the site capital Investment Committee reviewing and assessing capital appropriations requests (CARs) are fit-for-purpose and right-sized. Articulates the business value created and overall value proposition to the site, regional and global SC, MAKE investment committees
- Owns asset Reliability elements from asset creation (system), PM design, spares strategy, to technical issues related to manufacturability
- Leads the Digital technical agenda in execution
- Owns Machine Safety
- Is responsible for developing department annual budgets, and monitoring/controlling budget performance. Ensures sound management of head count and expenses to meet approved spending plan and site functional targets
- Leads the local Maintenance Agenda and oversees adherence to best practices and processes as adopted across the Supply Chain (JJOS-Manage Site assets) and the Consumer Health Maintenance CoE.
- Engages, inspires, coaches and develops peers and subordinates toward the objectives of enhanced job performance, technical knowledge, career satisfaction, and professional development and growth.
- Is responsible for ensuring the ISA-95 level 1 and 2 systems and associated operation is compliant and fit for intended use in accordance with applicable standards and procedures throughout systems lifecycle
- Partners with MS&T Technology Strategy & Innovation team, Cluster leads and Enterprise in the design and delivery of appropriate contracts and agreements for contracted services, provided an adequate labor pool for all needed services
**Reliability & Maintenance**:
- Set and manage priorities for local Reliability & Maintenance organization to ensure delivering to KPI/targets to improve performance
- Oversee, optimize the site maintenance budgets, maintenance plans, long term equipment replacement plans, and spare part sourcing strategies
- Develop, institutionalize best practices and training related to root cause problem solving, preventive & predictive maintenance, parts room inventory mgmt etc.
- Collaborate with and contribute to the Maintenance Consumer Health Governance community
**CapEx Project & Portfolio M
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Ingenn è la società di Head Hunting unicamente focalizzata nella ricerca e selezione di profili tecnici e ingegneri .
The partner:Ricerchiamo una figura che si occupi di Direzione Lavori & Site Management in ambito industrial per prestigiosa e rinomata società multinazionale specializzata nella produzione, sviluppo e commercio di gas industriali e medicinali per ogni settore produttivo, dall’agroalimentare all’energia, dal chimico-farmaceutico all’elettronico, dal meccanico e metallurgico al vetro e cemento. In interfaccia costante con clienti che si occupano di microelettronica e semiconduttori, questa figura si occuperà di:
The role:- Supervisione delle attività di construction meccanica ed elettrica presso il cliente finale, comprendendo il coordinamento e la supervisione dei team coinvolti; l'installazione in questione verterà principalmente sia su macchinari che su utenze.
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- Gestione e supervisione della sicurezza di cantiere quando necessario.
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- Aver maturato almeno 2 anni di esperienza in ruolo affine e in contesto chimico, farmaceutico oppure oil&gas costituisce requisito fortemente preferenziale.
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#J-18808-LjbffrTbd Site Management Associate 2
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Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
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Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Are you a current ICON Employee? Please click here to apply:
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Tbd Site Management Associate 2
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Lavoro visualizzato
Descrizione Del Lavoro
Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
INSERT ADVERT TEXT
Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Are you a current ICON Employee? Please click here to apply:
link
Project Manager - Infrastrutture e Site Management
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Con la passione per la tecnologia e il talento, il gruppo composto da 50.000 ingegneri ed esperti digitali offre una profonda esperienza intersettoriale in 30 paesi tra Nord America, EMEA e APAC.
Akkodis vanta un’ampia esperienza e un forte know-how in settori tecnologici chiave come la mobilità, i servizi software e tecnologici, la robotica, i test, le simulazioni, la sicurezza dei dati, l'intelligenza artificiale e l'analisi dei dati.
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Nell’ottica di un potenziamento del team, ricerchiamo una figura di
**Project Manager - Infrastrutture e site management**
La risorsa, inserita all’interno del Team di un’importante azienda multinazionale operante nel settore Energy, possiede una solida esperienza nella gestione di progetti infrastrutturali complessi e un solido background sulle tematiche QHSE (Quality, Health, Safety, Environment). Abile nel coordinare tutte le fasi
del ciclo di vita del progetto, dalla pianificazione alla consegna, garantendo il rispetto dei tempi, dei budget e dei requisiti di qualità e integrando standard elevati di sicurezza, qualità e sostenibilità. Esperto nella gestione di team multidisciplinari e nella negoziazione con fornitori esterni e Clienti per ottenere risultati
ottimali. Capacità comprovata nel gestire rischi e imprevisti, mantenendo un'elevata attenzione ai dettagli senza perdere di vista gli obiettivi strategici.
Nello specifico, si occuperà delle seguenti attività:
- Gestione completa del ciclo di vita dei progetti infrastrutturali
- Implementazione e monitoraggio dei protocolli QHSE, assicurando il controllo dei processi
- Budgeting, schedulazione dei progetti e controllo dei costi
- Leadership e gestione di team multidisciplinari e fornitori
- Gestione dei rischi e problem solving
- Conoscenza approfondita delle best practice nel settore delle infrastrutture
- Conoscenza approfondita della normativa e delle best practice in ambito QHSE
- Gestione dei rischi per massimizzare la sicurezza in cantiere
- Negoziazione contrattuale con Clienti, fornitori e partner
- Comunicazione efficace con stakeholder interni ed esterni
**Requisiti**
Sono richieste le seguenti competenze:
- Esperienza di almeno 5 anni nel ruolo
- Gestione di progetti di infrastrutture e delle commesse relative alla fase di realizzazione
- Supervisione e coordinamento di un team multidisciplinare e gestione delle risorse
- Definizione dei requisiti del progetto, pianificazione delle risorse e monitoraggio dei progressi per garantire il rispetto dei tempi e dei budget stabiliti.
- Implementazione e controllo documentazione QHSE nelle fasi di progetto, compresa la fase di
cantiere.
- Implementazione di sistemi di gestione della qualità, audit interni e analisi delle prestazioni, assicurando la conformità con le normative e il miglioramento continuo dei processi.
- Gestione di risorse umane e materiali in linea con le normative QHSE, garantendo il rispetto dei requisiti regolamentari e delle migliori pratiche del settore
- Collaborazione con fornitori e partner esterni per negoziare contratti vantaggiosi e garantire la qualità dei servizi forniti
- Gestione delle relazioni con gli stakeholder per comunicare efficacemente i progressi del progetto e garantire l'approvazione e il supporto delle parti interessate.
- Rappresentano un plus:
- Certificazione ispettore ponti e viadotti almeno 2° livello
- Certificazioni come CSE, DL, CSP, Preposto, Dirigente per la sicurezza (ex DL 81/08)
- Certificazioni in Project Management (PMP, PRINCE2, black belt, etc.)
**Offerta**
Tempo Indeterminato
**Location**
Milano
Clinical Research Associate, Site Management - Italy
Inserito 27 giorni fa
Lavoro visualizzato
Descrizione Del Lavoro
Job Overview
Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.
Essential Functions
• Complete appropriate therapeutic, protocol and clinical research training to perform job duties.
• Gain experience in study procedures by working with experienced clinical staff.
• Under close supervision, perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with contracted scope of work and good clinical practices.
• Under close supervision, administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.
• Under close supervision, evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution.
• Under close supervision, ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with Good Clinical Practice (GCP) / International Conference on Harmonization (ICH) and local regulatory requirements.
• Under close supervision may support start-up phase.
• Under close supervision, create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.
• If applicable, learn key facets for successful development of project subject recruitment plan on a per site basis. Suggest ideas for improving site recruitment plan in line with project needs to enhance predictability. Assist in tracking subject site recruitment progress.
Qualifications
• Bachelor's Degree Degree in scientific discipline or health care preferred. Req
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• In possess of the local ministerial decree as per Italian requirements.
• Prior clinical experience preferred.
• Some organizations may require 2 years of clinical experience.
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
• Written and verbal communication skills including good command of English language.
• Organizational and problem-solving skills.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Advanced knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Knowledge of applicable protocol requirements as provided in company training.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at
#J-18808-LjbffrClinical Research Associate, Site Management - Italy
Inserito 5 giorni fa
Lavoro visualizzato
Descrizione Del Lavoro
Job Overview
Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.
Essential Functions
• Complete appropriate therapeutic, protocol and clinical research training to perform job duties.
• Gain experience in study procedures by working with experienced clinical staff.
• Under close supervision, perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with contracted scope of work and good clinical practices.
• Under close supervision, administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.
• Under close supervision, evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution.
• Under close supervision, ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with Good Clinical Practice (GCP) / International Conference on Harmonization (ICH) and local regulatory requirements.
• Under close supervision may support start-up phase.
• Under close supervision, create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.
• If applicable, learn key facets for successful development of project subject recruitment plan on a per site basis. Suggest ideas for improving site recruitment plan in line with project needs to enhance predictability. Assist in tracking subject site recruitment progress.
Qualifications
• Bachelor's Degree Degree in scientific discipline or health care preferred. Req
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• In possess of the local ministerial decree as per Italian requirements.
• Prior clinical experience preferred.
• Some organizations may require 2 years of clinical experience.
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
• Written and verbal communication skills including good command of English language.
• Organizational and problem-solving skills.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Advanced knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Knowledge of applicable protocol requirements as provided in company training.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at
#J-18808-LjbffrSii il primo a saperlo
Informazioni sulle ultime novità Site management Posti di lavoro;/Posti Vacanti nella Italia !
Clinical Research Associate, Site Management - Italy
Inserito 14 giorni fa
Lavoro visualizzato
Descrizione Del Lavoro
Job Overview
Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.
Essential Functions
• Complete appropriate therapeutic, protocol and clinical research training to perform job duties.
• Gain experience in study procedures by working with experienced clinical staff.
• Under close supervision, perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with contracted scope of work and good clinical practices.
• Under close supervision, administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.
• Under close supervision, evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution.
• Under close supervision, ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with Good Clinical Practice (GCP) / International Conference on Harmonization (ICH) and local regulatory requirements.
• Under close supervision may support start-up phase.
• Under close supervision, create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.
• If applicable, learn key facets for successful development of project subject recruitment plan on a per site basis. Suggest ideas for improving site recruitment plan in line with project needs to enhance predictability. Assist in tracking subject site recruitment progress.
Qualifications
• Bachelor's Degree Degree in scientific discipline or health care preferred. Req
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• In possess of the local ministerial decree as per Italian requirements.
• Prior clinical experience preferred.
• Some organizations may require 2 years of clinical experience.
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
• Written and verbal communication skills including good command of English language.
• Organizational and problem-solving skills.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Advanced knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Knowledge of applicable protocol requirements as provided in company training.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at
#J-18808-LjbffrClinical Research Associate, Site Management - Italy
Inserito 25 giorni fa
Lavoro visualizzato
Descrizione Del Lavoro
Clinical Research Associate, Site Management - Italy page is loadedClinical Research Associate, Site Management - Italy Apply locations Milan, Italy time type Full time posted on Posted 2 Days Ago job requisition id R
Job Overview
Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.
Essential Functions
• Complete appropriate therapeutic, protocol and clinical research training to perform job duties.
• Gain experience in study procedures by working with experienced clinical staff.
• Under close supervision, perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with contracted scope of work and good clinical practices.
• Under close supervision, administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.
• Under close supervision, evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution.
• Under close supervision, ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with Good Clinical Practice (GCP) / International Conference on Harmonization (ICH) and local regulatory requirements.
• Under close supervision may support start-up phase.
• Under close supervision, create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.
• If applicable, learn key facets for successful development of project subject recruitment plan on a per site basis. Suggest ideas for improving site recruitment plan in line with project needs to enhance predictability. Assist in tracking subject site recruitment progress.
Qualifications
• Bachelor's Degree Degree in scientific discipline or health care preferred. Req
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• In possess of the local ministerial decree as per Italian requirements.
• Prior clinical experience preferred.
• Some organizations may require 2 years of clinical experience.
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
• Written and verbal communication skills including good command of English language.
• Organizational and problem-solving skills.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Advanced knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Knowledge of applicable protocol requirements as provided in company training.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at
About UsIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
#J-18808-LjbffrClinical Research Associate, Site Management - Italy
Inserito 21 giorni fa
Lavoro visualizzato
Descrizione Del Lavoro
Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.
**Essential Functions**
- Complete appropriate therapeutic, protocol and clinical research training to perform job duties.
- Gain experience in study procedures by working with experienced clinical staff.
- Under close supervision, perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with contracted scope of work and good clinical practices.
- Under close supervision, administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.
- Under close supervision, evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution.
- Under close supervision, ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with Good Clinical Practice (GCP) / International Conference on Harmonization (ICH) and local regulatory requirements.
- Under close supervision may support start-up phase.
- Under close supervision, create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
- If applicable, learn key facets for successful development of project subject recruitment plan on a per site basis. Suggest ideas for improving site recruitment plan in line with project needs to enhance predictability. Assist in tracking subject site recruitment progress.
**Qualifications**
- Bachelor's Degree Degree in scientific discipline or health care preferred. Req
- Equivalent combination of education, training and experience may be accepted in lieu of degree.
- In possess of the local ministerial decree as per Italian requirements.
- Prior clinical experience preferred.
- Some organizations may require 2 years of clinical experience.
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
- Written and verbal communication skills including good command of English language.
- Organizational and problem-solving skills.
- Effective time and financial management skills.
- Ability to establish and maintain effective working relationships with coworkers, managers and clients.
- Advanced knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Knowledge of applicable protocol requirements as provided in company training.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
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