Clinical Research Associate

2 giorni fa

Lazio, Italia Jr Italy A tempo pieno

Social network you want to login/join with:CliniRx has a number of CRA positions available to support a global study in Q******.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—most notably small to mid-size enterprises facing unique challenges.Our presence includes key markets such as the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia.------------------------------------------------------------Primary Purpose:We are seeking skilled CRAs to ensure the timely and high-quality delivery of site monitoring activities in line with our Site Monitoring Plan (SMP).Key Responsibilities: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 therapeutic areas to expand our clinical network.Continuous Skill Development:Regularly improve technical and soft skills to enhance performance and project outcomes.Work Relations: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.Value Added:Your commitment to quality and timely execution of monitoring activities is crucial for the successful delivery of our projects.Key Success Factors:Timely, high-quality 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 in site monitoring within clinical research.Skills:Strong knowledge of ICH GCP and applicable clinical trial regulations; excellent communication skills; ability to multitask and perform under tight deadlines.#J-*****-Ljbffr

  • Clinical Research Associate

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    Lazio, Italia Barrington James A tempo pieno

    Freelance Clinical Research Associate (CRA) – Cardiology Medical Devices12-Month Freelance Contract (Direct with Sponsor)Location: Italy (must be based in Italy)Start Date: ASAPAbout the RoleWe are seeking an experienced Freelance Clinical Research Associate (CRA) with a strong background in cardiology medical devices to support a high-priority clinical...

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    Lazio, Italia Informatica Software A tempo pieno

    Clinical Research Associate All Level-Home Based-South KoreaICON plc is a world-leading healthcare intelligence and clinical research organization.We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Clinical...

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    Lazio, Italia Informatica Software A tempo pieno

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    Lazio, Italia Opis A tempo pieno

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    Lazio, Italia Tfs Healthscience A tempo pieno

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    Lazio, Italia Jr Italy A tempo pieno

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    Lazio, Italia Jr Italy A tempo pieno

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    Lazio, Italia Parexel A tempo pieno

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    4 giorni fa

    Lazio, Italia Teleflex A tempo pieno

    POSITION SUMMARYThe Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable regulatory standards (MDR, ISO *****, ICH / GCP guidelines, Teleflex procedures and IRB / EC policies and procedures).The Senior CRA conducts monitoring visits as identified by the...