20 annunci per il ruolo di associate - arcore, lom (recruiting in corso)

Clinical Research Associate, Site Management - Italy
IQVIA —Milano, Lombardia
- 33.900 € - 61.700 € all'anno
- Part-time
- Microsoft Powerpoint
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Ecolab Inc. —Vimercate, Lombardia
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Project Manager, Water treatment and reuse/recycle
Ecolab Inc. —Vimercate, Lombardia
- 55.600 € - 83.500 € all'anno
- Tempo pieno
- AutoCAD
- Gestionale
- Inglese
- Partecipazione agli utili
Apprentice Commercial Excellence
Ecolab Inc. —Vimercate, Lombardia
- 29.000 € - 31.000 € all'anno
- Tempo pieno
- Microsoft Powerpoint
- Microsoft Word
- Spagnolo
Visiting Associate (fixed term contract), Italy
Boston Consulting Group —Milano, Lombardia
- 29.800 € all'anno
- Tempo pieno
- Microsoft Powerpoint
- Microsoft Excel
- Inglese
Oliver Wyman - Data&Analytics - Associate Team Leader - Milan
Oliver Wyman —Milano, Lombardia
- 49.000 € - 75.000 € all'anno
- Tempo pieno
- Inglese
- Laurea magistrale
- SQL
Retail Business Consultant
Bridgestone —Vimercate, Lombardia
- 31.266 € - 49.500 € all'anno
- Tempo pieno
- Microsoft Powerpoint
- Microsoft Excel
- Microsoft Outlook
IT Support Apprentice
Ecolab Inc. —Vimercate, Lombardia
- 29.000 € - 31.000 € all'anno
- Tempo pieno
- Remoto
- Spagnolo
- Informatica
- Servizio clienti
Solution Architect - GHT
Ecolab Inc. —Vimercate, Lombardia
- 63.200 € - 94.800 € all'anno
- Tempo pieno
- Vendite
- Ingegneria
- Laurea magistrale
Equipment Service Coordinator - Italy
Ecolab Inc. —Vimercate, Lombardia
- 49.100 € - 73.500 € all'anno
- Tempo pieno
- Gestionale
- Inglese
- Microsoft Office
Training Manager
Ecolab Inc. —Vimercate, Lombardia
- 59.500 € - 89.200 € all'anno
- Tempo pieno
- Vendite
- Leadership
Senior Solution Architect
GFT Technologies SE —Milano, Lombardia
- 60.000 € - 75.000 € all'anno
- Remoto
- Gestionale
- Project management
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Application Engineer Paper
Ecolab Inc. —Vimercate, Lombardia
- 41.400 € - 62.200 € all'anno
- Tempo pieno
- Inglese
- Microsoft Office
- Laurea triennale
Visiting Associate
Impacta Strategy —Milano, Lombardia
- Microsoft Powerpoint
- Microsoft Excel
- Gestionale
Candidatura rapida
Business Development Manager - GHT
Ecolab Inc. —Vimercate, Lombardia
- 63.200 € - 79.000 € all'anno
- Tempo pieno
- Vendite
- Laurea triennale
CTM/Sr CTM - EMEA - FSP
Thermo Fisher Scientific —Milano, Lombardia
- Tempo pieno
- Remoto
- Inglese
- Microsoft Office
- Laurea triennale
Associate, Industrial Practice
Spencer Stuart —Milano, Lombardia
- 40.000 € - 60.000 € all'anno
- Tempo pieno
- Gestionale
- Inglese
- Project management
Senior Associate, IT R&D Engineer
Alfasigma Group —Milano, Lombardia
- 36.000 € - 48.000 € all'anno
- Gestionale
- Inglese
- Microsoft Office
Human Resources, Recruiting and Legal Talent Coordinator
Latham & Watkins LLP —Milano, Lombardia
- 35.000 € - 45.000 € all'anno
- Tempo pieno
- Inglese
- Competenze analitiche
- Laurea triennale
- Convenzioni aziendali

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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

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Voglio ricevere gli ultimi avvisi Job Alert per il ruolo di associate nella seguente località: arcore, lom

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