Senior Clinical Research Associate
Job Summary
To support the CDS Ophthalmology team, the part-time Freelance Senior Clinical Research Associate will conduct site monitoring visits and ensure compliance with clinical protocols and regulatory requirements while working fully remote.
Key Responsibilities:
- Take ownership of investigative sites from activation through study close-out
- Conduct various site visits including Qualification, Initiation, Monitoring, and Close-Out Visits
- Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements
Required Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field
- 3-5 years of independent clinical monitoring experience as a CRA, with at least 1 year in Ophthalmology
- Experience with Gene Therapy or Advanced Therapy programs
- Strong knowledge of ICH-GCP and clinical trial regulations
- Fluency in Dutch and professional proficiency in English
Complete Job Description
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