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Descripción de la vacante
An established industry player is seeking skilled Clinical Research Associates (CRAs) to support a global study launching in Q1 2025. This role is pivotal in ensuring the timely and high-quality delivery of site monitoring activities. As part of a rapidly expanding contract research organization, you will collaborate with diverse teams and contribute to the success of clinical trials across various therapeutic areas. Your expertise in site management and commitment to quality will be essential in navigating the complexities of clinical research, making this an exciting opportunity for professionals looking to make a significant impact in the field.
Formación
- 1-4 years of experience in site monitoring within clinical research.
- Strong knowledge of ICH GCP and clinical trial regulations.
Responsabilidades
- Ensure adherence to the Site Monitoring Plan and quality standards.
- Assist in identifying new potential clinical sites.
Conocimientos
Educación
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CliniRx has several CRA positions available to support a global study starting in Q1 2025. We are expanding rapidly and offer multiple permanent opportunities to join our team on a global scale. Ideally, candidates will have a background in CROs with experience across various 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 needs for emerging biotech and pharmaceutical companies, especially 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.
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 is vital for the successful delivery of our projects.
- Timely, high-quality site monitoring activities.
- Prompt report generation and submission.
- 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 and work under demanding timelines.
* El índice de referencia salarialse calcula en base a los salarios que ofrecen los líderes de mercado en los correspondientes sectores. Su función es guiar a los miembros Prémium a la hora de evaluar las distintas ofertas disponibles y de negociar el sueldo. El índice de referencia no es el salario indicado directamente por la empresa en particular, que podría ser muy superior o inferior.