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Parexel FSP is hiring a Site Activation Partner in Mexico, Argentina or Brazil Candidates must have at least 2 years of experience in start-up working with US/Canada. This is a 7-month temporary assignment with the potential to transition into a full-time role.
The Site Activation Partner (SAP) is responsible for leading or supporting operational activities from start- up to close-out, for assigned studies and investigator sites to ensure compliance with study timelines and in accordance with prevailing laws, Good Clinical Practices, and Client standards. Responsibility within a country and may span over more than 1 country depending on the geographical region and business needs.
Organizational Relationships:
Reports to Parexel-assigned Line Management with day-to-day direction from Client; refer to Organizational Chart for details regarding assigned role and associated reporting structure.
Primary Responsibilities:
Clinical Trial Site Activation




Initiate and coordinate activities and essential documents management during start-up towards the compilation of a high-quality Investigator Initiation Package (IIP) leading to approval for site initiation
Register investigator sites and Client stakeholders in Client registries and systems as required. Update and regularly maintain the registry with accuracy and have it inspection ready
Work directly and interact with investigator sites to confirm readiness for site start-up by reviewing study site profile ready in Shared Investigator Platform (SIP) or reviewing/completing critical information Sheet inclusive of but not limited to Investigator Initiation Packages (IIP) essential documents components, Site contracts contacts, clinical supply shipment information, payment information, IRB submission and status
Take the lead to resolve issues or concerns and timely escalation of Site issues where applicable
Prepare, validate and submit regulatory documents such a

📌 Site Activation Partner I (Argentina)
🏢 Parexel
📍 Argentina