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Clinical Research Associate
i dettagli
CliniRx have a number of CRA positions available to support a global study in Q1 2025.
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.
Essential Skills Experience:
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.
Clinical Research Associate
CliniRx
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