Clinical Trial Associate Job at ICON | Apply Now
A rare chance has emerged for aspiring candidates seeking a Clinical Trial Associate role at ICON plc, a leading healthcare intelligence and clinical research organization. This remote position offers an opportunity to contribute to clinical research activities while ensuring compliance with study protocols and regulatory requirements.
- Position: Clinical Trial Associate
- Location: Blue Bell, USA – Remote
- Reference Number: JR159329
- Department: Clinical Trial Support
About ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization. The company is dedicated to fostering an inclusive environment that drives innovation and excellence in clinical development. With a commitment to shaping the future of clinical research, ICON operates globally, providing a range of services to support the pharmaceutical and biotechnology industries.
Clinical Trial Associate Job Description
As a Clinical Trial Associate at ICON, the successful candidate will support the management and monitoring of clinical trial sites. Responsibilities include ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines while contributing to clinical research activities and collaborating with cross-functional teams.
Eligibility Criteria
The ideal candidate will possess relevant clinical research experience along with the following qualifications and skills:
- Bachelor’s degree in a relevant field such as life sciences, or clinical research.
- Experience in clinical research, site management, or monitoring, with a solid understanding of clinical trial processes and GCP guidelines.
- Strong organizational and project management skills, with the ability to handle multiple priorities and deadlines.
- Excellent analytical skills and attention to detail, with a focus on maintaining high-quality standards.
- Exceptional communication and interpersonal skills, with the ability to build and maintain effective relationships with site personnel and cross-functional teams.
- Willingness to travel as required (approximately 25%).
Clinical Trial Associate – Key Responsibilities
- Coordinating monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues.
- Assisting in the preparation and review of regulatory documents, ensuring all site activities are compliant with GCP and applicable regulations.
- Collaborating with cross-functional teams to facilitate effective communication and support for trial sites throughout the study lifecycle.
- Tracking site performance metrics, analyzing data, and providing reports to enhance site management efficiency.
- Participating in training initiatives and mentoring junior staff to support their development in clinical trial management.
With a strong commitment to clinical excellence and innovation, ICON plc presents a compelling opportunity for qualified candidates to contribute to impactful clinical research. Interested individuals interested in this Clinical Trial Associate opportunity are encouraged to apply at the earliest to seize this opportunity.
