Advance your career with Parexel FSP as a Clinical Study Administrator located in Mississauga, Ontario. This hybrid role focuses on coordinating clinical studies from initiation to closeout with vital document management tasks. The position requires you to assist with the administration of clinical studies while meeting ICH-GCP standards.

You will interface with investigators, manage essential documents, and ensure timely submissions to various regulatory bodies. Solid organizational and administrative skills are crucial for success in this role, which offers a blend of in office collaboration and work from home flexibility. Key Responsibilities:
Coordinate and administer clinical studies from start-up to closeout
Collect and track documents for regulatory submissions




Interface with investigators and service providers
Maintain local eTMF and ISF for inspection readiness
Support contract preparation and HCO/HCP payments Requirements:
High school qualifications or equivalent
Previous administrative experience in medical/life sciences
Strong organizational and administrative skills
Computer proficiency and good English skills
Willingness to train others on procedures Leverage your organizational and document management skills to ensure clinical study success at Parexel FSP in Mississauga.

📌 Clinical Study Administrator In Mississauga
🏢 Parexel
📍 Mississauga