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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, 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.
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Primary Purpose:
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).
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 various therapeutic areas to expand our clinical network.
* Continuous Skill Development: Regularly enhance technical and soft skills to improve 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 adherence to quality standards and timelines will be crucial for the efficient delivery of our projects and overall success.
Key Success Factors:
* 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.
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