20 annunci per il ruolo di 3 x software quality assurance engineers/senior software engineers arduino, turin, italy - milano, lom (recruiting in corso)

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Oliver Wyman – Data & Analytics - Senior Analyst - Italy
Oliver Wyman —Milano, Lombardia
- 43.000 € - 52.000 € all'anno
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- Inglese
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Industry Technical Consultant - Water Reclamation
Ecolab Inc. —Milano, Lombardia
- 63.200 € - 94.800 € all'anno
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Quality Assurance Manager, Regional Quality
GE HEALTHCARE —Milano, Lombardia
- 66.400 € - 91.300 € all'anno
- Medicina
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Implementation Specialist - Italy
Base.com —Milano, Lombardia
- 35.000 € - 45.000 € all'anno
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- Sistemi ERP
Candidatura rapida
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Software Engineer, iOS Core Product - Milan, Italy
Speechify —Milano, Lombardia
- 30.000 € - 80.000 € all'anno
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11 ore
Software Engineer, Data Infrastructure & Acquisition - Milan, Italy
Speechify —Milano, Lombardia
- 30.000 € - 80.000 € all'anno
- Remoto
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- Laurea magistrale
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Quality Assurance position in TIGET Clinical Lab (SR-Tiget, Milan)
Ospedale San Raffaele srl —Milano, Lombardia
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Senior L&H Client Manager & Actuary (Hybrid; m/f/x/d), Milano (IT)
Swiss Re —Milano, Lombardia
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4 giorni
Mid/Senior Solution Architect - Italy
MULTIVERSE COMPUTING —Milano, Lombardia
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UNIQLO Management Candidate - Graduate Programme Italy - 2026
UNIQLO —Milano, Lombardia
- 36.600 € all'anno
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- Inglese
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Full Stack Engineer - Arduino, Turin, Italy
Qualcomm —Milano, Lombardia
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Vitrolife Group —Milano, Lombardia
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Eurofins Italy —Milano, Lombardia
- Tempo pieno
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- Microsoft Word
- Microsoft Excel
- Gestionale
Candidatura rapida
Senior QA Auditor - GCP Audits
IQVIA —Milano, Lombardia
- 47.500 € - 71.300 € all'anno
- Part-time
- Microsoft Word
- Gestionale
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Clinical Research Associate II - Multi-Sponsor
Parexel —Milano, Lombardia
- Microsoft Word
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Technical Sales Representative - Milan and Rome
Dell Technologies —Milano, Lombardia
- 44.560 € - 61.160 € all'anno
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- Laurea triennale
- Competenze organizzative

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Clinical Research Associate, Site Management - Italy

IQVIA -
Milano, Lombardia

Candidati adesso

Dettagli della posizione

Part-time
33.900 € - 61.700 € all'anno

Qualifiche

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Gestionale
Inglese
Laurea magistrale

Descrizione completa della posizione

Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
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. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.
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, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications

Master's Degree in Life Sciences.

In possession of CRA certification according to Ministerial requirements.
Completion of CRA training program or prior monitoring experience.
Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
Good therapeutic and protocol knowledge as provided in company training.
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.

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 https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is €33,900.00 - €61,700.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Candidati adesso

Perfeziona la tua ricerca

3 x software quality assurance engineers/senior software engineers arduino, turin, italy offerte - milano, lom

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Voglio ricevere gli ultimi avvisi Job Alert per il ruolo di 3 x software quality assurance engineers/senior software engineers arduino, turin, italy nella seguente località: milano, lom

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