DO NOT APPLY - TEST REQ - CRG - (DO NOT USE) CRA (Level II) - Shanghai China

Thermo Fisher Scientific ·📍 Shanghai · 5 dagen online
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DO NOT APPLY - TEST REQ - CRG - (DO NOT USE) CRA (Level II) - Shanghai China

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Ready to make an impact as a Clinical Research Associate II? Join our global team to coordinate and monitor clinical trials, ensuring compliance with protocols and regulations. Contribute to groundbreaking research and collaborate with leading pharmaceutical and biotech companies. Take the next step in your clinical research career with us.
We are looking for a FSP CRA (Level II) to perform and coordinate clinical monitoring and site management processes. Key responsibilities include ensuring protocol and regulatory compliance, and managing documentation. Ideal candidates will have experience in clinical research monitoring and strong communication skills.
Embrace the role of a Clinical Research Associate II and play a vital role in advancing clinical trials for leading pharmaceutical companies. Utilise your expertise in clinical monitoring, ICH-GCP compliance, and site management to ensure data integrity and regulatory adherence. Grow your career in a dynamic, global environment with opportunities for professional development.
Step into the role of Clinical Research Associate II at Thermo Fisher Scientific and help advance global health. Conduct and coordinate clinical monitoring, ensure regulatory compliance, and support investigational sites. Join a team dedicated to delivering life-changing therapies and making a positive impact worldwide.
We are seeking a FSP CRA (Level II) to perform and coordinate clinical monitoring and site management processes, ensuring protocol and regulatory compliance. Key responsibilities include monitoring investigator sites and managing documentation. Ideal candidates will have experience in clinical research monitoring and a background in life sciences or nursing.
Become part of our team as a Clinical Research Associate (Level II), where you will monitor clinical trial sites, ensure protocol and regulatory compliance, and manage documentation. Ideal candidates have experience in clinical research monitoring and strong organizational and communication skills.
Step into the role of Clinical Research Associate II at Thermo Fisher Scientific. Perform and coordinate clinical monitoring and site management, ensuring compliance with protocols and regulations. Join a global team dedicated to advancing clinical research and improving health outcomes. Apply your expertise to make a meaningful impact in clinical trials worldwide.
Step into the role of Clinical Research Associate II and contribute to impactful clinical trials across the globe. You will coordinate site management, ensure regulatory compliance, and support investigational sites while working with leading pharmaceutical and biotech companies. Join us to advance your career in clinical research.
Step into the role of Clinical Research Associate II at Thermo Fisher Scientific and help advance global health outcomes. Conduct clinical monitoring, ensure regulatory compliance, and collaborate with investigational sites. Join us in making a positive impact through research, development, and delivery of life-changing therapies.
Step into the role of Clinical Research Associate II at Thermo Fisher Scientific and help advance global health outcomes. Conduct clinical monitoring, ensure regulatory compliance, and collaborate with investigational sites. Join us in making a positive impact through research, development, and delivery of life-changing therapies.

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