Study Start Up
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- Trial MaintenanceAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global 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 Study Start Up Associate I at ICON, you will facilitate the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
Your role will involve delivering site start-up and activation work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
Assisting in the preparation and submission of regulatory documents,



such as clinical trial applications and ethics committee submissions.
Coordinating with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.
Maintaining accurate and up-to-date records of regulatory submissions and approvals.
Supporting study teams in the development of study documents, including protocols, informed consent forms, and investigator brochures.
Participating in study start-up meetings and providing input on regulatory requirements and timelines.
Your Profile:
You will bring relevant site start-up and activation experience, along with the following qualifications and skills. Required qualifications and experience: Bachelor's degree in life sciences or a related field.
Experience in submission, substantial and non-substantial amendments Mexico.
Previous experience in clinical research or regulatory affairs preferred, but Nt required.
Strong attention to detail and organizational skil

📌 Study Start Up Associate (Cataluña)
🏢 Icon Clinical
📍 Cataluña