CRA II – Sponsor Dedicated

Syneos Health

. Perform site qualification, site initiation, interim monitoring, site management and close-out visits, on-site or remotely .

Posted 11/10/2026full-timeRemote • SpainMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in site management, regulatory compliance, and clinical monitoring, with a strong focus on Good Clinical Practice and ICH Guidelines. Capable of effectively communicating with site personnel and managing site-level activities to ensure project objectives are met.

Highest-signal resume keywords

Site ManagementGood Clinical Practice/ICH GuidelinesClinical MonitoringRegulatory ComplianceData Collection

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Site QualificationSite InitiationSource Document ReviewPharmacovigilanceChart AbstractionClinical Data AccuracyProtocol DeviationsInvestigational Product ReviewAction Plan DevelopmentMonitoring Activity Documentation

Soft Skills

Excellent CommunicationPresentation SkillsInterpersonal Skills

Tools & Technologies

Trial Master FileClinical Monitoring Software

Certifications & Qualifications

Bachelor’s DegreeRN in a Related Field

Industry Keywords

ImmunologyCardiologyPulmonary HypertensionOphthalmologyLipids

About the role

Key responsibilities & impact

Perform site qualification, site initiation, interim monitoring, site management and close-out visits, on-site or remotely
Evaluate site and site staff performance and provide recommendations and action plans
Ensure regulatory, ICH-GCP/GPP and protocol compliance
Verify informed consent processes and protect subject/patient confidentiality
Assess subject/patient safety, protocol deviations and pharmacovigilance issues
Conduct source document review and verify clinical data accuracy and completeness
Resolve queries remotely and on site within agreed timelines
Review investigational product inventory, storage, dispensing and administration as applicable
Review Investigator Site Files and reconcile them with the Trial Master File
Document monitoring activities through letters, reports, logs and project documents
Support subject/patient recruitment, retention and awareness strategies
Track observations, site status and action items to resolution
Manage site-level activities and communications to meet project objectives, deliverables and timelines
Act as liaison with study site personnel and ensure site team training and compliance
Prepare for and attend investigator, sponsor and clinical monitoring meetings and training sessions
Support audit readiness and audit follow-up actions
Support sites throughout the study lifecycle, including site identification through close-out
Perform chart abstraction and data collection for Real World Late Phase studies
Collaborate with sponsor affiliates, medical science liaisons and local country staff
Train junior staff when requested
Identify and communicate out-of-scope activities
Suggest potential sites based on local treatment patterns, patient advocacy and healthcare provider associations

Requirements

What you’ll need

Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience
3-4 years of experience as CRA
Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
Good computer skills and ability to embrace new technologies
Experience in Immunology, Cardiology, Pulmonary Hypertension, Ophthalmology or Lipids
Excellent communication, presentation and interpersonal skills

Benefits

Comp & perks

Career development and progression
Supportive and engaged line management
Technical and therapeutic area training
Peer recognition
Total rewards program
Inclusive culture
Reasonable accommodations, when appropriate