Job Description
CliniRx has multiple Clinical Research Associate (CRA) positions available to support a global study in Q1 2025. We are expanding rapidly and offer permanent opportunities to join us on this project. Candidates with a CRO background and experience across multiple therapeutic areas are preferred.
As a global contract research organization (CRO), we provide diverse 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, with a presence in 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 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 various 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 on 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 is crucial for the efficient delivery and success of our projects.
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 in site monitoring within clinical research.
* Skills: Strong understanding of ICH GCP and clinical trial regulations; excellent communication skills; ability to multitask under demanding timelines.
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