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CliniRx CRA Positions - Global Study Q1 2025
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.
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
1. 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.
2. Site Management Compliance: Manage sites according to the SMMP and relevant regulations to minimize Quality Assurance (QA) audit observations.
3. Site Identification: Assist in identifying new potential sites across various therapeutic areas to expand our clinical network.
4. 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 adherence to timelines is vital for the successful delivery of our projects.
Key Success Factors
* 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.
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