Clinical Trial Research Associate
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Clinical Trial Research Associate
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Global drug and device development services
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As an IHCRA at ICON, you will support the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies.
What You Will Do:
You will take responsibility for clinical trial monitoring deliverables, applying your skills to ensure quality and efficiency.
Key responsibilities include:
What You Will Be Doing:
Responsible for controlling the contract full details.
Lead the contract negotiation, and manage site payments.
Good experience with VeeVa Systems
Knowledge of Ariba, Apex, RGPS and Grant Plan
Coordinating the day-to-day operations of clinical studies, including site management, participant recruitment, and data collection.
Ensuring compliance with Good Clinical Practice (GCP) and regulatory guidelines throughout the study lifecycle.
Providing training and support to site staff and investigators on study protocols and operational procedures.
Your Profile:
Advanced degree in a relevant field such as life sciences, nursing, or healthcare administration.
Extensive experience in clinical study coordination or clinical trial management, preferably within the pharmaceutical or biotechnology industry.
Strong understanding of clinical trial processes, regulatory requirements, and GCP.
Excellent organizational skills and attention to detail, with the ability to manage multiple studies simultaneously.
Strong communication and interpersonal skills, with the ability to work collaboratively with diverse teams and stakeholders.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply
This company provides consulting, development, and commercialization support for drugs and medical devices through a global network of offices. Its team across 53 countries offers end-to-end services, from strategy and regulatory work to manufacturing and market access, helping clients shorten development time, lower costs, and raise quality. It differentiates itself with wide geographic reach and a clear focus on reducing time to market and cost while leveraging deep experience across many therapeutic areas. Its goal is to help clients accelerate the development of life-saving products and improve quality of life by delivering reliable information, practical solutions, and solid performance.
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