Study Start Up Associate I
About this role
Study Start Up Associate I
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.
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