Site Activation Lead - Clinical Trials

Parexel; United States; Remote; USD 90,000 - 130,000; Full time

Job summary

Parexel is seeking professionals to support clinical site activation and regulatory submissions across multiple countries. You will coordinate essential documents, ensure regulatory compliance, and maintain study files throughout the trial lifecycle.

Ideal candidates have clinical research experience, strong GCP knowledge, and excellent communication. The role involves collaboration with cross-functional teams and potential international travel to support site initiation.

Qualifications

• Experience in clinical site management or activation is preferred.
• Fluent communication in English; Turkish and English skills noted as helpful in education section.

Responsibilities

• Initiate and coordinate site activation activities and essential documents.
• Prepare regulatory submissions and maintain TMF/update life cycle documents.
• Support site ethics and regulatory submissions and align with country requirements.
• Coordinate with client and internal teams to ensure timely site activation and study conduct.
• Communicate with study teams and investigators to provide updates and resolve issues.

Skills

Clinical research

GCP knowledge

Documentation

Communication

Team collaboration

Education

Bachelor's degree or equivalent

Life sciences background

Tools

CTMS

eISF/ Florence

Shared Investigator Platform

Microsoft Office

Job description

Parexel is seeking professionals to support clinical site activation and regulatory submissions across multiple countries. You will coordinate essential documents, ensure regulatory compliance, and maintain study files throughout the trial lifecycle.

Ideal candidates have clinical research experience, strong GCP knowledge, and excellent communication. The role involves collaboration with cross-functional teams and potential international travel to support site initiation.