Site Activation Coordinator
On-site
Core
Coordinate regulatory submissions for clinical studies in Brazil, preparing documents for ethics and competent authorities.
Role type
Junior Regulatory Submissions Coordinator
Builds
Regulatory submission packages for clinical trials
Domain
Clinical Research / Life Sciences
Required skills
Regulatory submission preparation, Document quality control, Deadline management, ANVISA (RA) submissions, Biosafety commission (CTNBio) submissions, Microsoft Office, English fluency
Preferred skills
Master's/PhD, Regulatory surveillance strategy, 1-4 years regulatory experience
Technologies
Microsoft Office
Responsibilities
Collect vital documents for ethics submissions, Prepare study documents for competent authorities, Support managers on deadlines, Conduct quality control of documents, Provide compliance advice
Seniority
Entry-level / Junior
