Clinical Study Administrator

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. Strong organizational and administrative skills are crucial for success in this role, which offers a blend of on-site collaboration and remote work 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.
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