Senior Clinical Research Associate – Oncology

Parexel

Senior Clinical Research Associate managing clinical trials in oncology for Parexel. Conducting site management, monitoring, and ensuring patient safety across studies.

Posted 5/22/2026full-timeRemote • 🇬🇧 United KingdomSeniorWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan and applicable laws, Good Clinical Practices
Manage operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through database lock
Interface with the study team, facilitate information flow between team members and vendors
Monitor site level AEs and SAEs, collaborate with Drug Safety Unit and follow-up with investigators

Requirements

What you’ll need

Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations
Minimum 3.5 years relevant experience in clinical research site monitoring (preferably in Oncology)

Benefits

Comp & perks

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ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical trial methodologiessite monitoringGood Clinical PracticesStudy Monitoring Planadverse events monitoringserious adverse events monitoringdata managementregulatory compliance

Soft Skills

communicationcollaborationinformation flow facilitationteamwork

Certifications

Bachelor’s degree in life sciencesprofessional degree in life sciences