Lavori attuali relativi a Clinical Research Associate - Trento - Jr Italy
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Senior Clinical Research Associate – On-site
2 settimane fa
Trento, Italia JR Italy A tempo pienoA leading clinical research organization in Trento is seeking a Senior Clinical Research Associate. This role involves conducting monitoring visits, ensuring compliance with regulatory standards, and training Clinical Studies personnel. Ideal candidates will have more than 5 years of experience and a strong background in clinical trial monitoring....
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Senior Clinical Research Associate
2 settimane fa
Trento, Italia Altro A tempo pienoSocial network you want to login/join with:Senior Clinical Research Associate, trento col-narrow-leftClient: TeleflexLocation: Job Category: Other-EU work permit required: Yescol-narrow-rightJob Reference: Job Views: 2Posted: Expiry Date: col-wideJob Description: POSITION SUMMARY :The Senior Clinical Research Associate (Senior CRA) is responsible for...
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Clinical Research Associate
3 settimane fa
Trento, Italia Altro A tempo pienoSocial network you want to login/join with:CliniRx CRA Positions - Global Study Support Q1 2025 CliniRx has multiple CRA positions available to support a global study in Q1 2025. We are expanding rapidly and offer permanent opportunities to join us on a global study. Ideally, candidates will have a CRO background with experience across multiple therapeutic...
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Senior Clinical Research Associate
2 settimane fa
Trento, Italia JR Italy A tempo pienoSocial network you want to login/join with: Senior Clinical Research Associate, trento col-narrow-left Client: Teleflex Location: Job Category: Other - EU work permit required: Yes col-narrow-right Job Reference: Job Views: 2 Posted: Expiry Date: col-wide Job Description: POSITION SUMMARY : The Senior Clinical Research Associate (Senior CRA) is responsible...
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Senior Clinical Research Associate
2 settimane fa
Trento, Italia Altro A tempo pienoSocial network you want to login/join with: Senior Clinical Research Associate, trentocol-narrow-left Client:Teleflex Location:Job Category:Other - EU work permit required:Yes col-narrow-right Job Reference: Job Views:2 Posted: Expiry Date: col-wide Job Description:POSITION SUMMARY : The Senior Clinical Research Associate (Senior CRA) is responsible for...
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Senior Clinical Research Associate
2 settimane fa
Trento, Italia Altro A tempo pienoSocial network you want to login/join with:col-narrow-leftClient: TeleflexLocation: Job Category: Other-EU work permit required: Yescol-narrow-rightJob Reference: Job Views: 2Posted: Expiry Date: col-wideJob Description: POSITION SUMMARY :The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and conducting on-site and remote...
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Clinical trial manager
7 giorni fa
Trento, Italia Advanced Clinical A tempo pienoClinical Trial Manager – Italy | Advanced Clinical (FSP Model)Oncology focusedAdvanced Clinical is seeking an experienced Clinical Trial Manager to join our UK-based Functional Service Provider (FSP) team. This role will support global clinical studies and requires strong operational, vendor management, and monitoring oversight experience.Responsibilities...
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Senior CRA
2 settimane fa
Trento, Italia Altro A tempo pienoA medical device company in Trentino-Alto Adige is seeking a Senior Clinical Research Associate to perform both on-site and remote monitoring in compliance with regulatory standards. Candidates should have a minimum of 5 years' experience in clinical trial monitoring, along with strong organizational and interpersonal skills. This role promotes continuous...
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Trento, Italia Altro A tempo pienoA position for a UX Technologist at Digital Health Innovation Laboratory (DHILab)Join to apply for the A position for a UX Technologist at Digital Health Innovation Laboratory (DHILab) role at Fondazione Bruno Kessler - FBKFBK is a private research institution devoted to excellence in research in numerous disciplines and designated to the role of keeping the...
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Sr. Data Associate
1 settimana fa
Trento, Italia Amazon A tempo pienoAI is the most transformational technology of our time, capable of tackling some of humanity's most challenging problems.Amazon is investing in generative AI and the responsible development and deployment of large language models (LLMs) across all of our businesses.Come build the future of human-technology interaction with us.We are looking for those...
Clinical Research Associate
2 settimane fa
Social network you want to login/join with:CliniRx CRA Positions - Global Study Support Q******CliniRx has multiple CRA positions available to support a global study in Q******.We are expanding rapidly and offer permanent opportunities to join us on a global study.Ideally, candidates will have a CRO background with experience across multiple therapeutic areas.As a global contract research organization (CRO), we provide a diverse range of clinical development and resource solutions, including full-service CRO and functional service provider (FSP) models.We support clinical outsourcing for emerging biotech and pharmaceutical companies, especially small to mid-size enterprises facing unique challenges, with a presence in the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia.Primary PurposeWe 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 ResponsibilitiesDeliver on the Site Monitoring Plan:Understand the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality and timelines.Site Management Compliance:Manage sites according to the SMMP and relevant regulations to minimize QA audit observations.Site Identification:Assist in identifying new potential sites across various therapeutic areas to expand our clinical network.Continuous Skill Development:Regularly enhance technical and soft skills to improve performance and project outcomes.Work RelationsReport to the Manager of Clinical Operations for project, functional, and administrative matters.Collaborate with the site monitoring team, site personnel, HR, site leads, and administrative staff.Value AddedYour commitment to quality and timeliness is crucial for the successful delivery of projects and overall company success.Key Success FactorsTimely, high-quality site monitoring activities.Prompt report generation and stakeholder communication.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 clinical trial regulations; excellent communication skills; ability to multitask under demanding timelines.#J-*****-Ljbffr
