Senior Project Specialist in Clinical Trials

Join a partner company as a Senior Project Specialist focusing on clinical trials. This fully remote role requires bilingual capabilities to support significant research efforts in Canadian healthcare.

As a Senior Project Specialist, you will ensure the smooth coordination of clinical trials by managing critical documentation and adhering to regulatory compliance. Your expertise will be crucial in Trial Master File management and cross-functional collaboration, all while working independently in a remote environment. This position is designed for highly organized individuals ready to impact patient-focused therapies positively.

Key Responsibilities:

• Reconcile and manage Trial Master Files for accuracy

• Archive regulatory documents and clinical study essentials

• Support study startup activities and site coordination

• Monitor operational metrics and study timelines closely

• Lead project meetings with agendas and follow-ups

Requirements:

• 2–3+ years of Clinical Trial Assistant experience

• Hands-on Veeva Vault TMF management experience

• Strong document management and regulatory knowledge

• Bilingual proficiency in English and French is preferred

• Ability to manage multiple tasks effectively

Bring your detailed organizational skills and clinical trial knowledge to support innovative healthcare research.
#J-18808-Ljbffr