Social network you want to login/join with:
CliniRx has a number of CRA positions available to support a global study in Q1 2025.
We are expanding rapidly and have multiple permanent opportunities to join us on a global study. Ideally, candidates will have a CRO background with experience across multiple therapeutic areas.
As a global contract research organization (CRO), we offer diverse 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—particularly small to mid-size enterprises facing unique challenges—with 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 high-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 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 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.
#J-18808-Ljbffr