Senior Clinical Research Associate

Precision Medicine Group

. Monitor and own the progress of clinical studies at investigative sites .

Posted 9/21/2026full-timeRemote • SpainSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in monitoring and managing clinical studies in compliance with ICH-GCP and applicable regulations, with a strong focus on IVD, oncology, and infectious diseases. Proven ability to train and mentor junior staff while effectively interacting with clients and coordinating study activities across multiple European countries.

Highest-signal resume keywords

CRA Certification5+ Years CRA/SCRA ExperienceIVD ExperienceFluency in Spanish and EnglishClinical Study Monitoring

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study MonitoringRegulatory SubmissionsProtocol ComplianceStudy Setup CoordinationInvestigator IdentificationData ReportingSOP AdherenceClinical Trial ManagementProposal DevelopmentClient Presentations

Soft Skills

MentoringClient InteractionTeam CollaborationTraining

Certifications & Qualifications

CRA Certification

Industry Keywords

CROPharmaceuticalBiotechnologyMedical DeviceIn Vitro DiagnosticsOncologyInfectious DiseasesGastrointestinal StudiesEuropean Clinical TrialsDomestic Travel

About the role

Key responsibilities & impact

Monitor and own the progress of clinical studies at investigative sites
Ensure studies are conducted, recorded, and reported according to protocol, SOPs, ICH-GCP, applicable regulations and standards
Coordinate study setup and monitoring activities, including investigator identification, regulatory submissions, pre-study visits and initiation visits
Handle appropriately sized clinical trials
Support larger clinical study teams
Train and mentor junior staff members
Interact directly with clients
Initiate payments
Participate in proposal activities, including development and client presentations

Requirements

What you’ll need

4-year college degree or equivalent experience
Holder of CRA certificate
Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical device environment
Extensive experience in IVD (In Vitro Diagnostics), oncology, infectious diseases and gastrointestinal studies
Proven experience monitoring studies across multiple European countries
Availability for domestic travel including overnight stays, up to approximately 50–60% travel commitment
International travel may be required for some senior-level positions
Fluency in Spanish and English is required
Apply in English

Benefits

Comp & perks

Employees are empowered to make an impact
Meaningful client relationships
Career growth opportunities
Professional development
Collaborative and quality-focused environment
Equal opportunity employer
Reasonable accommodation available during the application process