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.

📌 Clinical Study Administrator in Mississauga
🏢 Parexel International
📍 Mississauga