Site Activation Partner
ICON · Istanbul, Turkey
Clinical OperationsFull-timeCompany career page
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Role summary
Study Start Up Associate position focused on facilitating clinical trial initiation and regulatory compliance. The role involves preparing regulatory submissions, coordinating approvals, maintaining documentation, and supporting study teams in a sponsor-dedicated model within a global clinical research organization.
What they're looking for
- Bachelor's degree in life sciences or related field
- Strong attention to detail and organizational abilities
- Excellent communication and interpersonal skills
- Ability to manage multiple tasks independently in fast-paced environment
- Clinical research or regulatory affairs experience preferred
- Willingness to travel approximately 5% as required
- Legal right to work in Turkey
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 and authorizations
- 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.