Local Start Up Specialist
Job Summary
Supporting local site start-up activities, the part-time Local Start Up Specialist Contractor will coordinate essential document collection and regulatory submissions for clinical trials while working remotely in the United States.
Key responsibilities
- Coordinate and track site start-up activities, ensuring timely updates in CTMS and (e)TMF
- Assist in the preparation and submission of regulatory and ethical documentation to relevant authorities
- Support the collection and review of essential documents, ensuring compliance with local regulations
Required qualifications
- Degree in Life Science, Healthcare, or Biological Science, or equivalent experience
- Minimum of 2 years of relevant clinical development experience
- Fundamental knowledge of GxP and local regulatory requirements
- Strong written and verbal communication skills in English
- Proficiency in Microsoft Word, Excel, and PowerPoint
Complete Job Description
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