Remote Site Activation Partner I

Parexel International; Canada; On-site; CAD 60,000 - 90,000; Full time

Job summary

Parexel International is seeking a Site Activation Partner I to lead or support clinical start-up activities for assigned studies and investigator sites. The role requires coordinating regulatory submissions and ensuring compliance with GCP and client standards across Canada with potential multi-country involvement.

The position is a 7-month temporary assignment with the potential to transition into a full-time role, and candidates must have at least 2 years of start-up experience and

Qualifications

• Minimum 2 years relevant experience in clinical site activation.
• Fluent in English; bilingualism (French) preferred for Canada.
• Experience with US/CAN regulatory processes and GCP standards.

Responsibilities

• Lead or support start-up activities from site activation to close-out.
• Coordinate regulatory documents and IIP/IRB submissions.
• Maintain Trial Master File and ensure study documents are audit-ready.
• Support and communicate with investigators, sponsors, and ethics committees.

Skills

Clinical research knowledge

GCP knowledge

Attention to detail

Independent worker

Team player

Time management

CTMS familiarity

eTMF familiarity

Travel willingness

Bilingual English/French

Education

Bachelor's degree in life sciences

Tools

CTMS

eTMF (Florence)

Shared Investigator Platform

Regulatory databases

Job description

Parexel International is seeking a Site Activation Partner I to lead or support clinical start-up activities for assigned studies and investigator sites. The role requires coordinating regulatory submissions and ensuring compliance with GCP and client standards across Canada with potential multi-country involvement.

The position is a 7-month temporary assignment with the potential to transition into a full-time role, and candidates must have at least 2 years of start-up experience and