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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 opportunities on a permanent basis 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. We have a presence in key markets including 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 alignment with our Site Monitoring Plan (SMP).
Key Responsibilities:

Deliver on the Site Monitoring Plan: Gain a comprehensive understanding of the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality 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 within various therapeutic areas to expand our clinical network.
Continuous Skill Development: Regularly enhance both technical and soft skills, applying them to elevate 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 executives.

Value Added:
Your adherence to the quality and timelines of the monitoring plan 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; ability to multitask and thrive under demanding timelines.

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