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CliniRx CRA Positions - Global Study Support 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. Ideal candidates will have a CRO background 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, particularly 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

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 for 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 will be critical for the successful delivery of our projects and overall organizational success.
Key Success Factors

Timely and high-quality execution of site monitoring activities.
Prompt generation and submission of reports to stakeholders.
Education: Bachelor’s or Master’s degree in a scientific discipline.
Experience: 1-4 years of site monitoring experience in clinical research.
Skills: Strong knowledge 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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