Study Start Up Associate I
ICON · Sao Paulo, Brazil
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Site Activation Partner role supporting clinical trial initiation in Brazil. Responsibilities include preparing regulatory submissions, coordinating approvals, and maintaining compliance documentation while collaborating with internal and external stakeholders to advance study start-up activities.
What they're looking for
- Bachelor's degree in life sciences or related field
- Study start-up or site activation experience in Brazil
- Strong attention to detail and organizational skills
- Excellent communication and interpersonal abilities
- Ability to manage multiple tasks independently in fast-paced environment
- Clinical research or regulatory affairs experience preferred
What you'll be doing
- Prepare and submit regulatory documents including clinical trial applications and ethics committee submissions
- Coordinate with stakeholders to obtain necessary approvals and authorizations for study initiation
- Maintain accurate records of regulatory submissions and approvals
- Support development of study documents including protocols and informed consent forms
- Participate in study start-up meetings and provide regulatory input on requirements and timelines
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.