We are currently seeking a Study Start Up Associate to join our diverse and dynamic team. As a Study Start Up Associate at ICON, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of inNvative treatments and therapies.
What you will be doing
? 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
? Bachelor's degree in life sciences or a related field.
? About 1 year plus CRA experience.
? Strong attention to detail and organizational skills.
? Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.
? Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment.