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CliniRx
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Job Description:
CliniRx has multiple CRA positions available to support a global study in Q******.
We are expanding rapidly and offer multiple permanent opportunities to join us on a global study.
Candidates ideally should 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 for emerging biotech and pharmaceutical companies, especially small to mid-size enterprises, with a presence in the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia.
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Primary Purpose:We seek skilled CRAs to ensure the timely and high-quality delivery of site monitoring activities in line 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 quality and adherence to timelines.
Site Management Compliance:Manage sites according to the SMMP and relevant regulations to minimize QA audit observations.
Site Identification:Assist in identifying new potential sites across therapeutic areas to expand our clinical network.
Continuous Skill Development:Regularly improve technical and soft skills to enhance 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 adherence to quality and timelines is crucial for efficient project delivery and overall success.
Key Success Factors:
Timely and high-quality site monitoring activities.
Prompt report generation and stakeholder communication.
Education:Bachelor's or Master's degree in a scientific discipline.
Experience:1-4 years in site monitoring within clinical research.
Skills:Strong understanding of ICH GCP and clinical trial regulations; excellent communication skills; ability to multitask and work under demanding timelines.
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