Study Start Up Associate II (German-Speaker)
ICON · Warsaw, Poland +6 more
Clinical OperationsFull-timeCompany career page
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Role summary
ICON seeks a Study Start Up Associate II to facilitate clinical trial initiation across multiple European and African locations. The role involves regulatory document preparation, stakeholder coordination, and support for study team development, requiring fluency in English, German, and French or Romanian.
What they're looking for
- Professional fluency in English and German plus French or Romanian
- 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
- 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 internal and external stakeholders to obtain necessary approvals 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 advise on regulatory requirements and timelines
Privacy & handoff
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