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Insegnante per Aiuto Compiti - Versioni di latino
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Operaio/a di Produzione (legge 68-99)
ADECCO ITALIA S.p.A.
Clinical Research Associate
Résumé du poste
An established industry player is seeking skilled Clinical Research Associates (CRAs) to ensure timely and high-quality site monitoring for a global study. This role offers a unique opportunity to contribute to clinical development in a dynamic environment, supporting biotech and pharmaceutical companies. With a commitment to quality and adherence to timelines, the successful candidates will play a crucial role in the execution of site monitoring activities. Join a forward-thinking organization that values continuous skill development and collaboration, and make a meaningful impact in the clinical research field.
Qualifications
- 1-4 years of experience in site monitoring within clinical research.
- Strong understanding of clinical trial regulations.
Responsabilités
- Deliver on the Site Monitoring Plan ensuring adherence to quality standards.
- Manage sites and minimize Quality Assurance audit observations.
- Assist in identifying new potential sites across therapeutic areas.
Connaissances
Formation
CliniRx has a number of CRA positions available to support a global study in Q1 2025.
We are expanding rapidly and have multiple permanent opportunities to join us on a global study. Ideally, candidates will come from a CRO background with experience across multiple therapeutic areas.
As a global contract research organization (CRO), we offer a diverse range of clinical development and resource solutions, reflecting both full-service CRO and functional service provider (FSP) models. We support clinical outsourcing needs for emerging biotech and pharmaceutical companies—particularly small to mid-size enterprises facing unique challenges—and have a presence in key markets including the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia.
We are seeking skilled CRAs to ensure the timely and high-quality delivery of site monitoring activities in accordance with our Site Monitoring Plan (SMP).
- Deliver on the Site Monitoring Plan: Understand the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality standards and timelines.
- Site Management Compliance: Manage sites according to the SMMP and relevant regulations to minimize Quality Assurance (QA) audit observations.
- Site Identification: Assist in identifying new potential sites across various therapeutic areas to expand our clinical network.
- Continuous Skill Development: Regularly improve technical and soft skills to enhance performance and project outcomes.
- Report to the Manager of Clinical Operations regarding project, functional, and administrative matters.
- Collaborate with the site monitoring team, site personnel, HR, site leads, and administrative staff.
Your commitment to quality and adherence to timelines will be crucial for the successful delivery of our projects and overall organizational success.
- Timely and high-quality execution of site monitoring activities.
- Prompt report generation and submission to stakeholders.
- Education: Bachelor’s or Master’s degree in a scientific discipline.
- Experience: 1-4 years of experience in site monitoring within clinical research.
- Skills: Strong understanding of ICH GCP and applicable clinical trial regulations; excellent verbal and written communication skills; ability to multitask and perform under demanding timelines.
* Le salaire de référence se base sur les salaires cibles des leaders du marché dans leurs secteurs correspondants. Il vise à servir de guide pour aider les membres Premium à évaluer les postes vacants et contribuer aux négociations salariales. Le salaire de référence n’est pas fourni directement par l’entreprise et peut pourrait être beaucoup plus élevé ou plus bas.
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