Site Activation Partner I
ICON · Warsaw, Poland
Clinical OperationsFull-timeCompany career page
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Role summary
Site Activation Partner I facilitates the initiation of clinical trials at ICON Strategic Solutions, ensuring regulatory compliance and supporting study start-up activities. The role involves preparing regulatory documentation, coordinating approvals, and collaborating with internal and external stakeholders to advance clinical research.
What they're looking for
- Bachelor's degree in life sciences or related field
- Strong attention to detail and organizational skills
- Excellent communication and interpersonal abilities
- Ability to manage multiple tasks independently in fast-paced environment
- Willingness to travel approximately 5% as required
- Previous clinical research or regulatory affairs experience preferred
What you'll be doing
- Assist in preparation and submission of regulatory documents 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 study teams in developing protocols, informed consent forms, and investigator brochures
- Participate in study start-up meetings and provide regulatory guidance 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.