57 Posti di lavoro per Construction Planner in Italia

The Human Technopole Foundation (HT) is an interdisciplinary research institute, created and supported by the Italian government, whose aim is to develop innovative strategies to promote human health and healthy aging through a multidisciplinary and integrated approach, combining genomics, computational biology, structural biology, neuroscience and health data science. HT scientists work together to enable interdisciplinary research and to create an open, collaborative environment to help promote life science research nationally and internationally. In line with its mission to serve the research community at large, HT operates National Facilities, specifically aimed at making HT's technologies, methods and tools available to the national scientific community.

The Human Technopole Foundation is looking for a Fit-out Planner .

The Fit-out Planner is the key interface between CDFM area, Scientific Operations and research areas to collect specifications and requirements for laboratories and facilities implementation, evaluate the impacts and technically support the whole design and installation phase.

Human Technopole, located in Milan MIND Area and counts more than 20.The next stage of development will double the current size and will open multiple services to other national institutions .

Periodically collect specifications and requirements for laboratories implementation from Scientific Operations, laboratory and facility managers, National Platforms managers and technicians;

Support the digitalization and monitoring of the entire process to track evolving research needs or recurring issues, enabling early identification of design impacts and installation timing across construction works;

Contribute to the development of a multi-year laboratory implementation plan aligned with HT's strategic objectives and integrated into the long-term CDFM construction and maintenance strategy;

Provide technical support throughout the design process—including CAD and BIM drafting of fit-out plans and layouts—from initial design award to feasibility studies, detailed design, and tender documentation for construction works;

Offer technical support during construction and commissioning phases to ensure laboratory spaces meet the specific requirements for scientific instrumentation, including ongoing checks on logistics, noise/vibration, and environmental parameters in accordance with technical specifications and pre-installation manuals;

Technical support for the implementation of the technical requirements necessary to install the scientific instrumentation during construction and commissioning phase. Constant check of logistic, noise & vibration and environmental parameters related to new research equipment to be compliant with technical sheets/pre-installation manual provided;

Monitor work progress and ensure timely communication and updates to end users;

Define standard technical requirements in collaboration with Scientific Operations and research departments for the design of new laboratories or revamping of existing ones;

Maintain and regularly update technical documentation related to laboratory fit-outs.

Technical Diploma;

Minimum of 3 years' experience in a similar role within research, hospital, university, or pharmaceutical environments, R&D;

Proficiency in AutoCAD;

Proven experience working on projects managed through BIM (Building Information Modelling);

Fluency in Italian (both written and spoken);

Proficient in English, with strong communication skills in both written and verbal formats.

Organizational and social skills :

Strong ability to coordinate and monitor activities efficiently;

Please apply online sending:

• a full CV in English;

• a motivation letter in English.

WHY HUMAN TECHNOPOLE?

Welfare plans

Italian language training for foreigners

Flexible working hours

Remote working policy

Support for relocation.

Contract offered: the Foundation reserves, however, the right not to proceed with the awarding of the above-described assignment due to the effect of supervening regulatory provisions and/or obstructive circumstances.

Valeo is a global tech company that designs innovative solutions to reinvent mobility. We are an automotive supplier partner to automakers and new mobility actors worldwide. Our vision is to invent greener and more secure mobility through solutions focused on intuitive driving and reducing CO2 emissions. We are leaders in our industry and recognized as one of the largest global innovative companies.

Valeo Group is one of the world's largest automotive suppliers, focused on innovative products, development, and customer satisfaction. Working with us means managing the most advanced and sophisticated technologies.

Our Pianezza plant is part of the Visibility Systems Business Group, responsible for developing and manufacturing lighting products and electronics. From adaptive lighting technologies to interior and exterior lighting solutions, Valeo constantly innovates to improve driver and passenger comfort and safety.

As a Site Management Controller at Valeo Pianezza, you will have the opportunity to work with leading car manufacturers in an international and multicultural environment.

Mission :

1. Organize and supervise the management control team at the entity level with support from the Site Financial Controller.
2. Focus on controlling industrial costs, standards & budgets, supply chain costs, improvement plans, inventories, and site investments.
3. Coordinate the preparation and analysis of reports such as daily and weekly indicators, the monthly green book, budget, and medium-term plans.
4. Contribute to understanding and validating financial performance and ensure the reliability of financial statements (MAF / IFRS compliance).
5. Support management control for the site.
6. Manage the controlling department to improve performance, efficiency, and profitability while complying with local laws and Valeo standards.
7. Alert the Financial Controller immediately in case of significant risks.
8. Supervise the preparation of reporting elements, budgets, and analyze monthly results, monitoring financial performance and KPIs.
9. Ensure accuracy of management control and costing information in the ERP system.
10. Ensure the reliability of site gross margin and expenses during closing processes.
11. Promote, explain, and control the Internal Control framework within the perimeter, and monitor improvement plans to mitigate risks.
12. Propose solutions for litigations between sites, product lines, and groups.
13. Conduct on-site management control reviews and pre-validate IAR / CAA.
14. Coordinate the analysis of transfer price regulations.
15. Contribute to Group Ethics & Compliance programs by applying and respecting the code of ethics and Valeo policies.

People management :

Support training and career development of controlling staff. Foster a proactive team environment and help identify high potentials.

Desired skills and experience :

• Degree in Economics or Management (Mandatory).
• More than 3 years of experience in similar roles.
• Successful previous experience in audit / controlling, including people management, complemented by operational finance experience.
• Good experience in finance & audit to manage responsibilities effectively.
• SAP knowledge.
• Strong communication skills, target orientation, decision-making ability, and capacity to work under pressure.

If you do not meet all the requirements, don't worry — we still want to meet you!

Join Valeo and discover our benefits! We offer:

• The chance to follow a personalized career path within a leading tech company.
• A comprehensive onboarding program and a dedicated buddy system to help you integrate.
• Continuous training opportunities.

Don't miss the opportunity to join us and be part of an international company committed to ethics, transparency, empowerment, professionalism, and teamwork. Is this you? We look forward to meeting you!

#J-18808-Ljbffr

Valeo is a global tech company that designs innovative solutions to reinvent mobility. We are an automotive supplier partner to automakers and new mobility actors worldwide. Our vision is to invent greener and more secure mobility through solutions focused on intuitive driving and reducing CO2 emissions. We are leaders in our industry and recognized as one of the largest global innovative companies.

Valeo Group is one of the world's largest automotive suppliers, focused on innovative products, development, and customer satisfaction. Working with us means managing the most advanced and sophisticated technologies.

Our Pianezza plant is part of the Visibility Systems Business Group, responsible for developing and manufacturing lighting products and electronics. From adaptive lighting technologies to interior and exterior lighting solutions, Valeo constantly innovates to improve driver and passenger comfort and safety.

As a Site Management Controller at Valeo Pianezza, you will have the opportunity to work with leading car manufacturers in an international and multicultural environment.

Mission :

1. Organize and supervise the management control team at the entity level with support from the Site Financial Controller.
2. Focus on controlling industrial costs, standards & budgets, supply chain costs, improvement plans, inventories, and site investments.
3. Coordinate the preparation and analysis of reports such as daily and weekly indicators, the monthly green book, budget, and medium-term plans.
4. Contribute to understanding and validating financial performance and ensure the reliability of financial statements (MAF / IFRS compliance).
5. Support management control for the site.
6. Manage the controlling department to improve performance, efficiency, and profitability while complying with local laws and Valeo standards.
7. Alert the Financial Controller immediately in case of significant risks.
8. Supervise the preparation of reporting elements, budgets, and analyze monthly results, monitoring financial performance and KPIs.
9. Ensure accuracy of management control and costing information in the ERP system.
10. Ensure the reliability of site gross margin and expenses during closing processes.
11. Promote, explain, and control the Internal Control framework within the perimeter, and monitor improvement plans to mitigate risks.
12. Propose solutions for litigations between sites, product lines, and groups.
13. Conduct on-site management control reviews and pre-validate IAR / CAA.
14. Coordinate the analysis of transfer price regulations.
15. Contribute to Group Ethics & Compliance programs by applying and respecting the code of ethics and Valeo policies.

People management :

Support training and career development of controlling staff. Foster a proactive team environment and help identify high potentials.

Desired skills and experience :

• Degree in Economics or Management (Mandatory).
• More than 3 years of experience in similar roles.
• Successful previous experience in audit / controlling, including people management, complemented by operational finance experience.
• Good experience in finance & audit to manage responsibilities effectively.
• SAP knowledge.
• Strong communication skills, target orientation, decision-making ability, and capacity to work under pressure.

If you do not meet all the requirements, don't worry — we still want to meet you!

Join Valeo and discover our benefits! We offer:

• The chance to follow a personalized career path within a leading tech company.
• A comprehensive onboarding program and a dedicated buddy system to help you integrate.
• Continuous training opportunities.

Don't miss the opportunity to join us and be part of an international company committed to ethics, transparency, empowerment, professionalism, and teamwork. Is this you? We look forward to meeting you!

#J-18808-Ljbffr

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:

1. 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.
2. Gestione della pianificazione di progetto in costante contatto con gli stakeholders coinvolti, monitoraggio costi, supervisione redazione fascicolo tecnico di progetto, verifica SAL.
3. Gestione e supervisione della sicurezza di cantiere quando necessario.
4. Gestione costante degli scambi di informazioni tecniche e non sia con i responsabili di progetto lato cliente, sia con le società fornitrici di attrezzature.

Mandatory skills:

1. Laurea e/o diploma tecnico conseguito in discipline meccaniche, elettriche oppure elettromeccaniche.
2. Aver maturato almeno 2 anni di esperienza in ruolo affine e in contesto chimico, farmaceutico oppure oil&gas costituisce requisito fortemente preferenziale.
3. Ottima conoscenza di strumenti CAD 2D e 3D.
4. Buona conoscenza della lingua inglese (livello B2 minimo).
5. Disponibilità a trasferte frequenti su territorio nazionale (principalmente zona Novara).
6. Una buona conoscenza delle procedure di qualità ISO9001 costituisce requisito preferenziale.

Location:

Caponago (MB)

#J-18808-Ljbffr

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:

1. 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.
2. Gestione della pianificazione di progetto in costante contatto con gli stakeholders coinvolti, monitoraggio costi, supervisione redazione fascicolo tecnico di progetto, verifica SAL.
3. Gestione e supervisione della sicurezza di cantiere quando necessario.
4. Gestione costante degli scambi di informazioni tecniche e non sia con i responsabili di progetto lato cliente, sia con le società fornitrici di attrezzature.

Mandatory skills:

1. Laurea e/o diploma tecnico conseguito in discipline meccaniche, elettriche oppure elettromeccaniche.
2. Aver maturato almeno 2 anni di esperienza in ruolo affine e in contesto chimico, farmaceutico oppure oil&gas costituisce requisito fortemente preferenziale.
3. Ottima conoscenza di strumenti CAD 2D e 3D.
4. Buona conoscenza della lingua inglese (livello B2 minimo).
5. Disponibilità a trasferte frequenti su territorio nazionale (principalmente zona Novara).
6. Una buona conoscenza delle procedure di qualità ISO9001 costituisce requisito preferenziale.

Location:

Caponago (MB)

#J-18808-Ljbffr

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-Ljbffr

Clinical Research Associate, Site Management - Italy

Join to apply for the Clinical Research Associate, Site Management - Italy role at IQVIA .

Engage in a structured training program to acquire the knowledge and skills necessary to independently conduct clinical monitoring visits in accordance with study protocols, standard operating procedures, good clinical practice, and regulatory requirements.

Essential Functions

• Complete therapeutic, protocol, and clinical research training to perform job duties.
• Gain experience in study procedures by working with experienced clinical staff.
• Perform site monitoring visits (selection, initiation, monitoring, and close-out) under close supervision, following scope of work and GCP guidelines.
• Administer protocol and study training to sites and maintain communication to manage expectations and issues.
• Evaluate site practices for quality and compliance, escalating issues as needed.
• Track regulatory submissions, recruitment, CRF completion, and data queries to manage study progress.
• Ensure site documents are properly filed and maintained per GCP/ICH and local regulations.
• Support start-up phases as needed.
• Document site management activities and findings, submitting reports and follow-up letters.
• Collaborate with study team members to support project execution.
• Assist in developing and tracking site recruitment plans to improve predictability.

Qualifications

• Bachelor's Degree in a scientific or healthcare discipline.
• Possession of local ministerial decree requirements per Italian law.
• Preferred: at least 1 year of clinical experience.
• Proficiency in Microsoft Word, Excel, PowerPoint, and familiarity with laptops, iPhones, and iPads.
• Good communication skills in English.
• Strong organizational and problem-solving skills.
• Effective time and financial management skills.
• Ability to build effective working relationships.
• Knowledge of GCP and ICH guidelines.
• Understanding of protocol requirements as per training.

IQVIA is a leading global provider of clinical research services and healthcare insights. Learn more at .

#J-18808-Ljbffr

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-Ljbffr

**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 in scientific discipline or health care
- In possession of local ministerial decree requirements as per Italian law.
- At least 1 year prior clinical experience preferred.
- 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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