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CliniRx have a number of CRA positions available to support a global study in Q******.
We are expanding at a rapid rate and have multiple opportunities on a permanent basis to join us on a global study.
Ideally you will come from a CRO background with experience across multiple therapeutic area's.
As a global contract research organization (CRO), we offer a diverse slate of clinical development and resource solutions reflecting both full-service CRO and functional service provider (FSP) models.
In supporting clinical outsourcing needs for emerging biotech and pharmaceutical companies—most notably small to mid-size enterprises facing unique challenges we offer our expertise with a presence in key markets including the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia
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Primary Purpose:We are seeking skilled CRA's to ensure the timely and qualitative 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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