Remote LATAM Site Activation Specialist (7-Month Contract)

Parexel International; México; Remote; MXN 860,000 - 1,290,000; Part time

Job summary

Parexel FSP is seeking a Site Activation Partner to lead or support start-up activities across Mexico, Argentina or Brazil. The role requires at least 2 years of start-up experience working with US/Canada and involves coordinating essential documents for site initiation under a 7-month temporary assignment with potential to transition to a full-time role.

You will manage regulatory submissions, IIP packages, and collaboration with study teams to ensure site readiness and regulatory compliance

Qualifications

• Minimum school diploma or Bachelor degree in life sciences.
• Experience with clinical site activation and start-up processes.
• Knowledge of ICH/GCP guidelines and regulatory requirements.

Responsibilities

• Initiate and coordinate site start-up activities and IIP documentation.
• Register investigator sites and maintain registry accuracy.
• Review readiness for site start-up using SIP and IIP components.
• Prepare regulatory documents and submissions within timelines.
• Collaborate with Study Team to ensure timely site activation.
• Maintain communication with Clients and Ethics committees.
• Support site activation in multiple countries as needed.
• Conduct training and ensure compliance with SOPs.

Skills

Clinical site activation

GCP / ICH knowledge

Regulatory submissions

Cross-functional coordination

Microsoft Office

SIP/eISF/eTMF familiarity

Education

Bachelor of Science in Life Sciences

Diploma/certificate in Life Sciences

Tools

CTMS

eISF/EDMS

Shared Investigator Platform (SIP)

Regulatory submission portals

Job description

Parexel FSP is seeking a Site Activation Partner to lead or support start-up activities across Mexico, Argentina or Brazil. The role requires at least 2 years of start-up experience working with US/Canada and involves coordinating essential documents for site initiation under a 7-month temporary assignment with potential to transition to a full-time role.

You will manage regulatory submissions, IIP packages, and collaboration with study teams to ensure site readiness and regulatory compliance