Hybrid Clinical Study Administrator Role

Enhance your career in clinical research as a Clinical Study Administrator at Parexel FSP in Mississauga, Ontario, with a hybrid work model. This role emphasizes the coordination and administration of clinical studies.

As a Clinical Study Administrator, you're expected to assist in managing study documents, ensuring timely submissions and compliance with regulatory requirements. Your previous experience in administration and skills in organization will be vital as you support a Local Study Team committed to delivering quality study outcomes.

Key Responsibilities:

• Help manage clinical studies from inception through closeout

• Prepare and submit essential documents to authorities

• Collaborate with external service providers during document collection

• Ensure eTMF and ISF compliance throughout the study

• Assist with internal meeting preparations and communications

Requirements:

• High school qualifications relevant to the job

• Experience in an administrative capacity within the medical field

• Strong organizational and computer skills

• Proficiency in English for document preparation and communication

• Flexibility to adapt to shifting priorities in a dynamic environment

Contribute your organizational acumen and dedication to Parexel FSP and help drive successful clinical trials.
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