Study Start Up Associate II
ICON · Sao Paulo, Brazil +1 more
Clinical OperationsFull-timeCompany career page
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
ICON seeks a Study Start Up Associate II to lead clinical trial initiation activities across Brazil and Mexico. The role involves managing regulatory submissions, coordinating stakeholder approvals, and supporting study teams on compliance requirements in a remote capacity.
What they're looking for
- Bachelor's degree in life sciences or related field
- Minimum 2 years clinical research or regulatory affairs experience with study start-up focus
- Strong knowledge of ICH-GCP and local regulatory requirements for clinical trials
- Excellent organizational and project management skills with multitasking ability
- Strong communication and interpersonal skills for cross-functional collaboration
- Willingness to travel approximately 5% as required
- Legal right to work in Brazil or Mexico
What you'll be doing
- Prepare and submit regulatory documents including clinical trial applications and ethics committee submissions
- Coordinate with internal and external stakeholders to obtain study initiation approvals
- Maintain comprehensive records of regulatory submissions, approvals, and correspondence
- Provide guidance to study teams on regulatory requirements and start-up best practices
- Participate in process improvement initiatives to enhance study start-up efficiency
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.