Senior Clinical Research Associate / Clinical Research Associate II – Oncology

Parexel

Senior Clinical Research Associate responsible for overseeing clinical trials and ensuring quality compliance. Engaging with investigator sites and managing study implementation in accordance to GCP.

Posted 6/29/2026full-timeRemote • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial monitoring and management, ensuring compliance with GCP, SMP, and regulatory standards while effectively communicating with investigator sites. Proficient in overseeing operational aspects of clinical trials, particularly in Oncology, to meet project goals and timelines.

Highest-signal resume keywords

Clinical Research Site MonitoringGood Clinical Practice (GCP)Oncology ExperienceProject ManagementFluency in English and Native Language

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementStudy Monitoring Plan (SMP)Regulatory ComplianceData ManagementOperational Oversight

Soft Skills

CommunicationInterpersonal SkillsProblem-Solving

Certifications & Qualifications

Valid Driver’s LicenseValid Passport

Industry Keywords

Clinical TrialsCROPharmaInvestigator SitesDatabase Lock

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Oversight of Monitoring Responsibilities and Study Conduct
Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and sponsor standards to achieve project goals, timelines and quality
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
During study conduct, serve as the primary point of contact for assigned investigator sites

Requirements

What you’ll need

Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) in a CRO or pharma organization
Must be fluent in English and in the native language(s) of the country they will work in
Valid driver’s license and passport required

Benefits

Comp & perks

Health insurance
Paid time off
Professional development opportunities