Senior Clinical Research Associate

Alira Health

Senior Clinical Research Associate conducting site monitoring for clinical trials at Alira Health. Leading team oversight and ensuring compliance and quality in clinical trial execution.

Posted 5/9/2026full-timeRemote • 🇪🇸 SpainSeniorWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Conduct site monitoring responsibilities for clinical trials
Provide oversight, leadership, and guidance in the management and execution of clinical trials to ensure compliance and quality
Ensure appropriate and timely investigator site visits
Review monitoring visit reports, conduct co-monitoring and evaluation visits as needed
Prepare consistently accurate and timely monitoring visit reports documenting site-related problems, resolutions, actions taken, protocol deviations, study progress, and enrollment status
Maintain regular contact with study sites to ensure protocol/GCP compliance, assess patient accrual rates, and respond to sponsor requests
Participate in internal, client/sponsor, scientific, and other meetings as required

Requirements

What you’ll need

US: BS/BA from an undergraduate program (life sciences or related discipline preferred)
US: 3 years of experience in the pharmaceutical/biotechnology/CRO industry, 2 years of clinical monitoring experience with 1 year of management experience
EU: Minimum 2 years of clinical monitoring experience in the pharmaceutical/biotechnology/CRO industry and ability to autonomously manage monitoring activities
US: Permanent authorization to work in the U.S.
EU: Certified Monitor in compliance with Italian CRO decree dated 15Nov2011
EU: Graduation in a scientific health field
Strong command of English, both written and verbal
Strong command of Local language, both written and verbal, in the country where monitoring activities are performed
Knowledge of clinical research, ICH GCP and local regulations
Knowledge of Regulatory and Ethical requirements

Benefits

Comp & perks

Professional development
Global travel
Flexible work programs

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical monitoringsite monitoringprotocol complianceGCP compliancereport writingdata evaluationproblem resolutionpatient accrual assessmentregulatory knowledgeethical requirements

Soft Skills

leadershipguidancecommunicationorganizational skillsinterpersonal skillsattention to detailproblem-solvingteam collaborationtime managementadaptability

Certifications

Certified MonitorBS/BA in life sciences or related discipline