Be Part of a Global Community
We are seeking a skilled Clinical Trial Start Up Associate to provide clinical trial capabilities in support of our clinical development efforts. As a key member of our team, you will ensure that investigator sites meet the necessary requirements to enroll study participants into clinical trials.
* Initiate and coordinate site activities, including the collection and submission of regulatory documents, customization and negotiation of informed consent documents, serve as the point of contact for a site's ERB and Competent Authority (where applicable), track and ensure site compliance to required training, and effectively drive timelines aligned with company priorities
* Communicate directly with sites to enable start-up and maintain an active collaboration with sites during maintenance and close-out
* Identify, communicate, and resolve issues
* Ensure country-specific regulatory and data privacy requirements are incorporated into submission documents and any other documents/systems
The ideal candidate has a Bachelor's degree preferably in a scientific or health-related field and understanding of the overall clinical development paradigm and the importance of efficient site activation. Native speakers with fluency in English are essential for this role.