Site Activation Partner
ICON · Canada
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Site Activation Partner role at ICON involving clinical trial initiation, regulatory compliance, and site start-up coordination. The position supports sponsor-dedicated models within a large clinical research organization, contributing to treatment development.
What they're looking for
- Bachelor's degree in life sciences or related field
- Strong attention to detail and organizational abilities
- Excellent communication and cross-functional collaboration skills
- Ability to manage multiple tasks independently in fast-paced environment
- Previous 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 approvals and authorizations for study initiation
- Maintain accurate records of regulatory submissions and approvals
- Support development of study documents such as protocols and informed consent forms
- Participate in study start-up meetings and provide input on regulatory requirements
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.