Remote Site Activation Specialist

Parexel; France; Sur place; EUR 42 000 - 65 000; Plein temps

Résumé du poste

Parexel seeks a Site Activation Partner for a 6-month temporary assignment in France. You will lead and support site activation and study start-up activities to ensure investigators are prepared, compliant, and activated on schedule.

Collaborating with investigator sites, regulatory stakeholders, and cross-functional teams, you will manage essential documents, regulatory submissions, and trial master file components to drive operational excellence across the study lifecycle.

Qualifications

• Experience in clinical site management or site activation.
• Bachelor's degree or equivalent required.
• Knowledge of regulatory submissions and CTMS platforms.
• Ability to collaborate across global teams and stakeholders.

Responsabilités

• Lead site activation activities to support timely start-up.
• Coordinate Investigator Initiation Packages and regulatory filings.
• Maintain trial master file and essential documents.
• Support audits and inspections and respond to findings.

Connaissances

Organizational skills

Documentation management

Stakeholder engagement

Regulatory compliance

Clinical research experience

Formation

Bachelor's degree

Outils

CTMS

eTMF

eISF

SIP

Description du poste

Parexel seeks a Site Activation Partner for a 6-month temporary assignment in France. You will lead and support site activation and study start-up activities to ensure investigators are prepared, compliant, and activated on schedule.

Collaborating with investigator sites, regulatory stakeholders, and cross-functional teams, you will manage essential documents, regulatory submissions, and trial master file components to drive operational excellence across the study lifecycle.