Elevate your career in clinical research with Parexel FSP as a Clinical Study Administrator in a hybrid role based in Mississauga, Ontario. This position focuses on coordinating study activities from start to close.
As a Clinical Study Administrator, you'll support the Local Study Team by managing essential study documents and ensuring compliance with ICH-GCP guidelines. Key skills include organizational and administrative expertise, along with proficiency in computer systems. Your role is crucial in maintaining study timelines and quality objectives.
Key Responsibilities:
• Coordinate study activities from start-up to closeout
• Manage submission of documents to EC/IRB and Regulatory Authorities
• Interface with Investigators and CRAs for data collection




• Maintain the local eTMF and ISF for compliance
• Prepare site-level contract materials as needed
Requirements:
• High school/Secondary school qualifications
• Administrative experience in medical/life sciences
• Proven organizational and administration skills
• Proficient in English, both written and spoken
• Valuable interpersonal skills for international teamwork
Bring your administrative skills and attention to detail to Parexel FSP and contribute to impactful clinical studies.
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📌 Clinical Study Administrator in Mississauga
🏢 Parexel International
📍 Mississauga