Senior Clinical Research Associate I - Oncology - Remote

Overview

The Senior Clinical Research Associate I at Parexel is responsible for field monitoring and management of clinical sites, specifically in oncology, ensuring compliance with regulatory guidelines.

In Short

• Responsible for monitoring and managing clinical sites in the Paris region.
• Act as liaison between in-house teams, vendors, and clinical sites.
• Develop strong relationships with investigative sites.
• Perform Pre-Study Site Visits and Site Initiation Visits.
• Provide training to site personnel on study protocols.
• Ensure compliance with CFR and GCP/ICH Guidelines.
• Prior monitoring experience in clinical trials is required.
• Oncology/haematology experience is essential.
• Proficiency in Microsoft Office and electronic systems is necessary.
• Join a team committed to improving global health.

Requirements

• BA/BS, or equivalent experience in pharmaceutical/biotech.
• RN or health care professional preferred.
• Prior monitoring experience is required.
• Oncology/haematology clinical trial experience is essential.
• FDA/EMA inspection experience preferred.
• Proficiency in CFR and GCP/ICH Guidelines is required.
• Experience in global clinical trials preferred.
• Proficiency in Microsoft Office Products and other electronic systems.

Benefits

• Opportunity to contribute to patient well-being.
• Work with a leading clinical research organization.
• Collaborate with a global team of professionals.
• Access to ongoing career development opportunities.
• Be part of a mission to improve global health.