Clinical Research Associate (In House) – ICON Careers | Life Science Job
Join ICON Strategic Solutions, part of ICON plc, a global leader in clinical research and healthcare intelligence. We are seeking an In-House Clinical Research Associate (IHCRA II) to support Sanofi Vaccines in Blue Bell. This exciting opportunity is ideal for professionals looking to advance their life science Job within a collaborative and innovative environment. At ICON careers, you’ll play a crucial role in managing clinical trials that shape the future of medical research and improve patient outcomes worldwide.
About ICON plc
ICON plc is a global leader in clinical research, providing high-quality solutions that accelerate drug and vaccine development. With operations in more than 40 countries, ICON partners with leading pharmaceutical, biotechnology, and medical device organizations to deliver impactful results. Through ICON careers, professionals in life science jobs and research roles contribute to innovations that improve lives worldwide.
Job Details
- Job Post: Sanofi Vaccines IHCRA
- Location: Remote
- Job ID: JR137655
About the Role
We are currently seeking a Site Management Associate II to join our diverse and dynamic team. As a Site Management Associate II at ICON, you will play a vital role in supporting the management and monitoring of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. You will contribute to the efficiency of clinical research operations by providing advanced support to site management teams and fostering strong relationships with site personnel.
Responsibility
- 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.
Requirements
- Bachelor’s degree in a relevant field such as life sciences, healthcare administration, 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.
Why Join ICON Careers?
Joining ICON careers means becoming part of a forward-thinking organization that empowers employees to make a tangible difference in global healthcare. You’ll work alongside industry experts on innovative projects that define the future of medicine. ICON offers extensive growth opportunities, flexible work options, and benefits that support your well-being and career progression in the life science job sector.
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