Senior Clinical Research Associate – Oncology Experience Required

Parexel

Senior Clinical Research Associate monitoring oncology clinical trials for Parexel, a global CRO. Ensuring site compliance, data integrity, patient safety, and inspection readiness across remote and on-site activities.

Posted 8/5/2026full-timeParis • 🇫🇷 FranceSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in regulatory compliance, particularly ICH-GCP and protocol adherence, while effectively managing oncology trial activities and stakeholder communications. Proficient in monitoring processes, data verification, and relationship-building within clinical research environments.

Highest-signal resume keywords

Oncology Trials ExperienceICH/GCP Guidelines KnowledgeInformed Consent VerificationEffective Communication SkillsSite Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Regulatory ComplianceClinical Data VerificationSource Document ReviewAdverse Event MonitoringProtocol Deviation ManagementData Query ResolutionMonitoring Plan ExecutionCase Report Form ReviewPharmacovigilanceRECIST Criteria Knowledge

Soft Skills

Networking SkillsRelationship-BuildingAdaptabilityInterpersonal SkillsPresentation Skills

Certifications & Qualifications

Bachelor’s DegreeRegistered Nurse (RN)

Industry Keywords

Clinical TrialsInvestigator MeetingsSite Staff Performance EvaluationClinical MonitoringStudy LogsProject Objectives ManagementTimelines ManagementLocal Language ProficiencyEnglish FluencySOPs/Processes Knowledge

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Ensure regulatory, ICH-GCP, protocol, and local-requirement compliance at investigator sites
Evaluate site and site-staff performance, communicate significant issues, and develop action plans
Verify informed-consent processes, subject confidentiality, safety factors, protocol deviations, and pharmacovigilance issues
Conduct on-site and remote monitoring activities according to the Monitoring Plan
Perform source document review and verify clinical data in Case Report Forms
Manage protocol deviations, data queries, adverse-event monitoring queries, and follow-up to resolution
Review investigational-product inventory, storage, dispensing, administration, labeling, import, release, and return
Document monitoring activities in reports, follow-up letters, communication logs, and project documents
Track observations, action items, data-entry timeliness, missing pages, queries, database-lock timelines, delegation logs, and training compliance
Check site facilities, equipment, supplies, and study logs
Collaborate with the Site Manager, site personnel, investigators, institutions, sponsor representatives, and global project teams
Prepare for and attend Investigator Meetings, sponsor meetings, clinical monitoring meetings, and clinic visits

Requirements

What you’ll need

Experience in oncology trials and RECIST criteria is essential
Bachelor’s degree or Registered Nurse (RN) in a related field, or equivalent combination of education, training, and experience
Proficiency in the local language is required
Advanced level or fluency in English is required
Knowledge of ICH/GCP Guidelines, applicable guidance, relevant regulations, and company SOPs/processes
Ability to conduct on-site and remote monitoring where permitted by country regulations
Networking and relationship-building skills
Effective communication with internal and external stakeholders
Ability to adapt to changing technologies and processes
Ability to overcome barriers during implementation of new processes and systems
Excellent verbal and written communication, presentation, and interpersonal skills
Ability to identify and build relationships with investigator site staff and stakeholders
Ability to manage site-level activities, communications, project objectives, deliverables, budgets, and timelines
Must be able to adapt quickly to changing priorities

Benefits

Comp & perks

🌐 Worldwide ❌ Jobs You've Hidden ⭐️ Saved Jobs ✅ Applied Jobs ✉️ Email Alerts 👤 Account Parexel Website LinkedIn All Job Openings 10,000+ employees Founded 1983 💼 Consulting 🏥 Healthcare 📦 Logistics 💰 Venture Round on 1990-01 Consulting
Healthcare
Logistics Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials. Senior Clinical Research Associate – Oncology Experience Required 🔥 17 minutes ago 🏢🏡 Paris – Hybrid ⏰ Full Time 🟠 Senior 🔬 Research Analyst 🗣️🇫🇷 French Required Apply Now Find Hiring Managers Customize resume + cover letter Report problem ☆ Save ☑️ Mark as applied ❌ Hide 📋 Description
Ensure regulatory, ICH-GCP, protocol, and local-requirement compliance at investigator sites
Evaluate site and site-staff performance, communicate significant issues, and develop action plans
Verify informed-consent processes, subject confidentiality, safety factors, protocol deviations, and pharmacovigilance issues
Conduct on-site and remote monitoring activities according to the Monitoring Plan
Perform source document review and verify clinical data in Case Report Forms
Manage protocol deviations, data queries, adverse-event monitoring queries, and follow-up to resolution
Review investigational-product inventory, storage, dispensing, administration, labeling, import, release, and return
Document monitoring activities in reports, follow-up letters, communication logs, and project documents
Track observations, action items, data-entry timeliness, missing pages, queries, database-lock timelines, delegation logs, and training compliance
Check site facilities, equipment, supplies, and study logs
Collaborate with the Site Manager, site personnel, investigators, institutions, sponsor representatives, and global project teams
Prepare for and attend Investigator Meetings, sponsor meetings, clinical monitoring meetings, and clinic visits 🎯 Requirements
Experience in oncology trials and RECIST criteria is essential
Bachelor’s degree or Registered Nurse (RN) in a related field, or equivalent combination of education, training, and experience
Proficiency in the local language is required
Advanced level or fluency in English is required
Knowledge of ICH/GCP Guidelines, applicable guidance, relevant regulations, and company SOPs/processes
Ability to conduct on-site and remote monitoring where permitted by country regulations
Networking and relationship-building skills
Effective communication with internal and external stakeholders
Ability to adapt to changing technologies and processes
Ability to overcome barriers during implementation of new processes and systems
Excellent verbal and written communication, presentation, and interpersonal skills
Ability to identify and build relationships with investigator site staff and stakeholders
Ability to manage site-level activities, communications, project objectives, deliverables, budgets, and timelines
Must be able to adapt quickly to changing priorities Apply Now 📊 Check your resume score for this job Improve your chances of getting an interview by checking your resume score before you apply. Check Resume Score Similar Jobs Research Analyst 🕒 June 12 PyData Paris 1 - 10 ₿ Crypto 💳 Fintech Website LinkedIn All Job Openings Research Analyst analyzing crypto markets using proprietary data at a global fintech company. Contributing to newsletters, reports, and expanding research reach across various platforms. 🏢🏡 Paris – Hybrid ⏰ Full Time 🟡 Mid-level 🟠 Senior 🔬 Research Analyst 🗣️🇫🇷 French Required View More Research Analyst Jobs 🌐 Worldwide Built by Lior Neu-ner. I'd love to hear your feedback — Get in touch via DM or support@remoterocketship.com Search Search Jobs by country Search jobs by city Search jobs by job title Search entry-level jobs Search junior-level jobs Search senior-level jobs Search jobs by tech stack Search jobs by contract type Search remote internships Search remote part-time jobs Remote jobs Anywhere in the World Companies Hiring Anywhere in the World Companies Hiring Sales People Anywhere in the World Companies Hiring Software Engineers Anywhere in the World Resources Advice Tips for finding remote jobs Interview questions and answers Resume examples Cover letter examples Post a job Affiliates About us Is Remote Rocketship legit? Privacy policy Terms of service Job board SEO course Remote Job Search MasterClass AI Apply Copilot OpenClaw job finder Find jobs using your resume Jobs by Country Remote jobs anywhere in the world (Worldwide remote jobs) Remote jobs United States Remote jobs Australia Remote jobs Brazil Remote jobs Canada Remote jobs France Remote jobs Ireland Remote jobs Germany Remote jobs Netherlands Remote jobs Spain Remote jobs UK Popular Jobs Remote data analyst jobs Remote customer support jobs Remote executive assistant jobs Remote marketing jobs Remote product designer jobs Remote product manager jobs Remote project manager jobs Remote recruiter jobs Remote sales jobs Remote software engineer jobs Jobs by Type Remote full-time jobs Remote part-time jobs Remote contract jobs Remote internship jobs Remote entry-level jobs Remote jobs with no experience required Remote junior jobs (1-3 years of experience) Digital nomad jobs Remote jobs with no degree required Freelance remote jobs Temporary remote jobs Remote jobs hiring now Stay at home mom jobs