Clinical Trial Submission Coordinator (España)

Clinical Trial Submission Coordinator (España)

02 oct
|
Icon Clinical Research
|
España

02 oct

Icon Clinical Research

España

POL-Start Up- HB
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s general expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
As a Principal, Study Start Up Associate at ICON, you will be responsible for leading the start-up activities for clinical trials, ensuring efficient site activation and compliance with regulatory requirements.
What You Will Do:
Your focus will be on coordinating site start-up and activation delivery, resolving issues, and developing team capability.
Key responsibilities include:
- Leading the preparation and submission of essential documents for regulatory approvals and site activation.
- Collaborating with cross-functional teams, including project management, clinical operations, and regulatory affairs, to streamline study start-up processes.
- Overseeing the identification and selection of clinical sites,



ensuring they meet project criteria and compliance standards.
- Providing guidance and support to study teams and sites during the start-up phase, fostering effective communication and collaboration.
- Staying current with industry regulations and trends to enhance start-up strategies and best practices.

Your Profile:
You will have solid site start-up and activation experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience in study start-up activities within the clinical research industry, with a strong understanding of regulatory requirements.
- Proven ability to manage multiple projects and prioritize tasks effectively in a fast-paced environment.
- Excellent organizational skills and attention to detail, with a commitment to de

📌 Clinical Trial Submission Coordinator (España)
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